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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role:

Project Manager - Laboratory IT and Data Integrity

Lead the planning and implementation of data integrity procedures and compliance working with a cross functional group within the organisation.
Facilitate the definition of project scope, goals and deliverables
Define project tasks and resource requirements.
Develop full-scale cross-functional project plans.
Plan and schedule project timelines
Qualification of laboratory equipment and associated software
Identify gaps in compliance across the laboratory in equipment and software qualification
Develop and Manage Risk Mitigation processes when gaps identified
Incorporate mitigation processes into standard operating procedures
Train laboratory staff on new processes post qualification
Track project deliverables using appropriate tools
Provide direction and support to project team
Communication of project progress to key stakeholders and senior management
Quality assurance
Constantly monitor and report on progress of the project to all stakeholders
Present reports defining project progress, problems and solutions.
Implement and manage project changes and interventions

Desirable attributes:

Laboratory experience (clinical / pharma / production)

Experience with automated laboratory equipment interfaced to a networked LIMS

Strong IT skills and knowledge

In depth experience of working with and configuration of a LIMS system

Experience in a laboratory or similar environment handling GXP data

Knowledge of laboratory equipment and associated software desirable

Knowledge of data integrity compliance advantageous

Knowledge of lab accreditation processes and standards

Experience of working with a quality management system including a robust CAPA process

Standard operating procedure creation including document control system desirable.

#LI-JS2

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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We are currently seeking a Project Manager, Laboratory to join our diverse and dynamic team. As a Project Manager, Laboratory at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.

What you will be doing

Ensure client satisfaction by acting as the Sponsor’s main contact person in all matters regarding ICON services including the day-to-day management of studies.

Attend and represent ICON at Sponsor meetings.

Manage 10-15 studies in accordance with Good Clinical Practice.

Communicate with Sponsor’s study progress in a responsible and professional manner and provide Sponsors with regular management reports.

Provide ICOLAB support to sponsor personnel.

Your profile

Bachelor's degree in a relevant field such as life sciences or healthcare.

Previous experience in project management within a laboratory or clinical research setting.

Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings.

Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines.

Detail-oriented with strong organizational skills to effectively manage study documentation and timelines.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

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Project Manager, Laboratory This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The Project Manager will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON Laboratory Services (ILS), including the setup and day-to-day management of studies, attend and represent ILS at Client meetings, manage studies in accordance with Good Clinical Practice, provide Clients with regular study updates and communicate study progress to Clients and PM Leadership in a responsible and professional manner, represent Project Management at internal interdepartmental meetings or interdivisional meetings within ICON, help train more junior PMs, act in an advisory role to those less experienced on the team, and work to enhance team tools and practices by actively recommending suggestions for improvements in efficiency, serve as the tactical site supervisor for project manager in the absence of a Team Lead for work related and administrative tasks and take on additional responsibilities to enhance the overall PM Team tools and Practices, as defined by Management. Overview of the Role

Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
Travel (approximately <20%) domestic and/or international
Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department.
Review newly assigned protocols and Amendments. Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate).
Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Prepare and QC clinical study specific materials.
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure.
Provide Sponsors with study management reports. Provide client with support on ICOLabs system. Inform team leader about study progress.
Proactively monitor study budget.
Set the timelines for and monitor the progress of shipment requests for storage samples and verify data.
Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Initiations.
Develop new tools, train new employees.
Performs additional relevant responsibilities as requested by management.

Role Requirements

Bachelor's degree or local equivalent in Science, Business or related Field
Minimum of 2 years of experience working in a clinical laboratory , clinical trials, or customer management/account management role in a life sciences related organization
Minimum of 1 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture.
Working familiarity with Word, Excel, PowerPoint
Excellent English Oral and Written Communications
Ability to Multi-Task
Ability to remain composed and professional in stressful situations, performing effectively with shifting priorities, workload and external pressures.
Excellent Presentation Skills
Organizational Agility
Ability to work with, and maintain the confidentiality of customer proprietary information.
Mastery in following established processes and use of all laboratory PM tools (e.g. configuring laboratory databases, tracking results, ordering supplies, )
Knowledge and familiarity with the clinical trials industry
Ability to successfully perform job functions with little or no supervision
Ability to effectively apply learned principles to broader situations

Benefits of Working in ICONOther than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career. What’s Next?Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

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Company Description

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 63 countries and about 63,000 staff.

Job Description

Eurofins Environment Testing is hiring for a Project Manager on location in Edison, New Jersey. Candidates should live within a commutable distance to the lab. Do you have 5 years of Project Management experience working in Environment? Apply today for a rewarding opportunity with the leader in Environment Testing.

This position is full-time, Monday - Friday, 1st shift on site in Edison, NJ Compensation (DOE) - salary mid $50-$65k Plus Full Benefits

The Project Manager I (PM I) is accountable for coordinating and managing clients’ projects through all phases of laboratory operations, including project set-up and maintenance, login review, communication of analytical issues, client account maintenance, reporting, invoicing, bottle orders, client pickups, and identification of work share facilities. The PM I role fosters and develops client relationships in support of the laboratory mission.

Essential Duties and Responsibilities:

Project Set-up

Project review in LIMS
Sets up project
Adds any project notes (special reporting and invoicing instructions, etc.)
Reviews project documentation
Adds any project documentation to central repository
Sets up client for Total Access
Manages purchase orders, task orders, contracts, and change order requests
Verified that lab compound lists and limits meet project requirements for new projects not quoted
Add any project specific limits/lists to LIMS
Deliverable assignment and delivery route
For new projects not quoted, confirms that EDD format is available (deliverable assignment and delivery route). Submits a helpdesk ticket for any new formats needed.
Communicates project details to operations
Initiates project kick off call with client and pertinent staff, if needed
Engages work share labs, service centers, and non-Eurofins locations as needed for new projects not quoted
Works with operations to ensure adequate capacity for incoming work (forecasting)
Provides updates to operations on upcoming work
Familiarity with state and national program requirements as it pertains to work mix
Create bottle orders
Schedules courier and field sampler, if needed
Confirms non-Eurofins subcontract labs area on the approved list and set-up as vendors for new work
Confirms non-Eurofins subcontract labs are on the approved list and set-up as vendors for existing work
Initiates approval process for any subcontract labs not on the approved list
Generates subcontract paperwork
Generates accounting software requisition when sending subcontract samples
Verifies that lab certification meets project requirements
Verifiers that lab compound lists and limits meet project requirements for new quotes
For new quotes confirms that EDD format is available (delivery assignment and delivery route). If new format is needed, submits a helpdesk ticket
Engages work share labs, service centers, and non-TA locations as needed for new quotes
Provides supporting documentation to client as needed (Contract list, bottle table with preservation, etc)

Sample Receipt

Communicates any issues to clients for duration of project
Manages incoming work for rush and short holds
Reviews log-in
Resolves log-in issues with client
Informs client of any log-in discrepancies
Sets samples to “available” after review
Sends client sample receipt confirmation
Reviews draft invoice
Confirms that any client needed information (Purchase order, project number, etc) is recorded in LIMS for invoicing

Reporting

Client specific report requirements
Reviews job list daily and manages due dates
Communicates any expected delays to clients before the job due date
Confirms any data anomalies (filtered>dissolved, deviations from historicals, etc) with operations before submitting to client
Reviews reports and EDDS before issuing to the client
Confirms correct report format and EDD format is used
Creates and issues final report by client due date
Issues final data packages
State reporting forms and submission
DMR forms
EDD checkers
Data upload
Compiles case narratives

Invoicing

Sets up delivery route
Reviews final invoice before issuing to client
Generates credit/debit memos as needed
Submits credit/debit memos for approval
Submits approved credit/debit memos to client, if needed
Submits revised invoices
Initiates follow up calls to confirm correct invoicing

Works with collections on A/R follow up
Regular review of A/R status

Client Set-up

Work with CSM to communicate lab capabilities to the client
Requests new client review
Confirms sales assignments with Business Development Manager
Takes new quote requests from clients
Reviews client contract requirements/coordinates review
Reviews purchase orders
Submits purchase orders for approval and returns approved orders to client
Follow up on client terms and credit limit

Account Maintenance

Follow up calls and visits with clients
Provides technical support as needed
Uses company resources to follow up on client requests
Familiarity with company capabilities and key contacts
Forward opportunities and leads to sales
Forecasts upcoming work
Asks for the next opportunity
Area of responsibility (air, regulations, etc)
Submits client complaints and participates in correction action/follow up as needed
Communicates client issues/complaints to sales
Follow up on client requests
Supports the follow up of quotes/bids for tracking purposes

Quotes & Proposals

Initiates project QAPP review with operations, QA, and subcontract labs as needed
Initiates technical support from operations as needed (special requests, method development, technical review, etc)
Quote generation and approvals
Reviews client quote requests for capabilities, certifications, scope
Confirms client contracts (if applicable) and pricing
Determines lab placement for the work
Confirms that lab certification meets project requirements
Confirms the lab compound lists and limits meet project requirements
Creates quotes
Submits quotes for approval
Sends quotes to client
Forecasts quotes
Provides QAPP/SOW information to the client as needed
Updates status in LIMS

Qualifications

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.

BS/BA in Chemistry/Sciences or related field (four years related experience may substitute for a degree
6-12 months of client relationship/customer service experience
Prefer some bench chemist or field experience
Requires additional lab training in methods and QA across multiple departments
Working knowledge of environmental regulations
Basic knowledge of the LIMS
Strong interpersonal, communication and problem solving skills
Effective time management
Strong organizational skills
Leadership skills
Multi-tasking
Adaptability and flexibility
Ability to ensure requirements for On-Time Delivery are met
Authorization to work in the United States indefinitely without restriction or sponsorship
Must be able to pass a pre-employment background check and drug screen
Attention to clients: demonstrates a desire to understand customer needs; listens to what customers are saying and asks questions as appropriate; demonstrates awareness of client goals. Follows up with clients during projects and following project completion; keeps clients up to date about decisions that affect them; seeks the comments, criticisms and involvement of clients; adjusts services based on client feedback
Technical familiarity: seeks information from a variety of sources in a variety of ways to respond to client’s technical questions about the project and to effectively communicate project status.
Customer service orientation: strives to meet customer expectations and takes responsibility to resolve client complaints. Provides prompt, efficient and personalized assistance to meet the requirements, requests, and concerns of customers; provides thorough, accurate information to answer customers’ questions and inform them of commitment times or performance guarantees; actively looks for ways to help customers by identifying and proposing appropriate solutions and/or services; establishes boundaries as appropriate for unreasonable customer demands.
Is pleasant, courteous and professional when dealing with internal or external customers; displays a good-natured, cooperative attitude; is calm and empathetic when dealing with hostile customers.
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.

Additional Information

We do not offer Visa Sponsorship for this role.

Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.

As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.

Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!

Find out more in our career page: https://careers.eurofins.com/

Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Edison, NJ, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":5,"item":{"@type":"JobPosting","title":"Strategic Project Manager - Global Laboratory Operations","datePosted":"2025-08-14","description":"

If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp as a Strategic Project Manager - Global Laboratory Operations.

In this role, you are part of the Project Management Office (PMO). In the Strategic Project Manager - Global Laboratory Operations role, you routinely manage different-scale, multifaceted, global projects bringing strategic advancement to laboratory operations.

In this role, the Strategic Project Manager - Global Laboratory Operations will provide internal and potentially external Clients with a central point of contact for assigned projects within Labcorp Clinical Trial Testing Solutions - PMO. The individual is accountable for leading the Program/Project teams to ensure that internal and external Client requirements and deliverables are met. This involves end-to-end management of a program/project, encompassing effective management of communications and use of the appropriate tools to ensure successful initiation, planning, execution, monitoring and completion of projects.

This position will be home based.

In more details, you will be responsible for the following:

Manage the day-to-day operational and tactical aspects of projects assigned
Responsible to create and manage detailed project plans
Responsible to report project status to team, management and stakeholders through regular status reports, management reports and communications meetings
Responsible to track project issues and ensure appropriate resolution working closely with the upper leadership
Responsible to hold formal project reviews with management to ensure successful project execution and customer satisfaction
Responsible to deliver projects successfully on time and on or under budget with regularity and predictability
Record actual labor utilization on the project and creates resource utilization forecasts
Assist the laboratory management and the wider organization in the following aspects of project planning
Project scope and change control processes
Manage the relationship within project teams, executive sponsors and all identified stakeholders
Motivate teams by presenting a vision and strategy for delivery
Negotiate on behalf of all project team members to ensure service delivery and team satisfaction
Effectively works with a diverse group of stakeholders in the organization
Project status updates
Project’s budget allocation, approval and management

What we are looking for:

Minimum of a Bachelors degree or country equivalent
Minimum 5 years of experience in Project Management, leading complex global projects
PMP certification
Experience leading complex strategic projects; managing or participation in IT projects are an advantage.
Demonstrated experience in team building, influencing and conflict resolution
Experience of working in a global multicultural environment
Previous experience of driving continuous improvement
Proven track record of successful project completion
Experience with project management tools including Microsoft Project and Office
Fluency in English
Proven leadership skills
Demonstrated strong customer service skills
Excellent written, verbal and interpersonal skills
Strong planning, organizational and problem solving skills
Demonstrated a high degree of initiative and ability to work collaboratively
This role can require some global travel when needed.

Thrive personally and professionally at Labcorp

Working at Labcorp, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s life.

In addition, Labcorp offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.

Get to know Labcorp

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.

Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

","hiringOrganization":{"@type":"Organization","name":"Labcorp","sameAs":"https://www.labcorp.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"GBR - Harrogate - Otley Road, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":6,"item":{"@type":"JobPosting","title":"Project Manager - Workplace - Laboratory Fitout Specialist","datePosted":"2025-08-18","description":"

About us

We have a proud heritage and a progressive future, providing world class drinking water and beautiful waterways from the mountains to the sea. We see the world is changing so we are changing too. Our people and their jobs are as diverse as the communities we serve.

Responsibilities include but are not limited to:

You will be responsible for executing project management processes across multiple projects, even when coordinators or vendor managers are involved.

Project Planning & Execution: Develop and execute project plans.

Scope Management: Plan, define, control, and verify project scope.

Cost Management: Forecast, report, control, estimate, and budget costs.

Time Management: Develop and control schedules.

Quality Management: Plan, control, and assure quality.

Risk/Issue Management: Identify, monitor, respond to, and plan for risks/issues.

Procurement: Plan purchases, manage procurement, and administer contracts.

Communication: Manage documents, plan communications, distribute information, and report performance.

You'll own key deliverables like project plans and schedules and refer unresolved issues to higher management. With high autonomy, you'll collaborate to define teams and achieve project outcomes, build strong relationships, set clear tasks, and ensure accountability and authority. Your leadership will foster team commitment and deliver agreed outcomes.

12-Month Fixed Term Role

Who are we looking for?

A degree in construction management or related discipline.

A qualification in one of the following. Property, building and construction, project management, engineering, architecture presentation skills and ability to take people on the change journey

Experience in project scheduling software (either Microsoft Project / Primavera)

Experience in project finance management software (SAP)

8+ years demonstrated industry experience

Demonstrated proficiency in identifying and managing avoidable project risks including reputational risk triggers, resolve issues in a proactive and timely manner; monitor and report progress.

NEC4 contract management and administration.

Ability to influence and manage 'difficult stakeholders’

Experience in the fitout of laboratory environment advantageous

Dive into Our Great Benefits:

Competitive Remuneration: We’ll ensure that your skills and contributions are valued and rewarded appropriately.

24/7 Wellbeing Support: Access for you and your family to free and confidential mental health and general health support through our EAP portal.

Discounted Private Health Insurance: Unlock affordable access to top-tier health coverage with our discounted insurance plans.

Fitness Passport: Achieve your physical fitness goals using our Fitness Passport, granting you access to a multitude of gyms and pools across NSW.

Applicants must be Australian Citizens or Permanent Residents.

Closing date: 1st September 2025

For more information, or to request an accommodation information, you can contact sunil.nagarajan@sydneywater.com.au

At Sydney Water, we are passionate about making a difference to the lives of our customers and communities. We have a proud heritage and progressive future providing world class drinking water and services that are vital to our customers’ quality of life and safeguarding Sydney’s future. We see the world is changing, so we are changing too.

Our vision is to create better lives through world-class services, and we believe that starts with our people. Our people and their jobs are as diverse as the communities we serve. Our diverse skills, mindsets and backgrounds work together on exciting and challenging projects that make a difference and help ensure Sydney remains one of the most iconic and liveable cities in the world.

We welcome and encourage applications from diverse backgrounds, including First Nations people, LGBTQIA+ people, people with disability, people with caring responsibilities, people from culturally and linguistically diverse backgrounds, and veterans.

As part of the application process, Sydney Water will be collecting your personal information to assess your suitability for the role. We will also use your personal information to establish a LiveHire talent profile in our Talent Community. We look at our Talent Community first when new opportunities come up when you apply for a role. Your personal information will be collected in accordance with LiveHire’s Terms, Privacy Policy and Sydney Water’s Privacy Collection Statement – Job Application. Please see the position description for the role’s full accountabilities.

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Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.

Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.

Job Description

Eurofins Environment Testing is searching for a Project Manager on location in Portland, Maine. Candidates should live within a commutable distance to the lab.

Do you have 5 years of Project Management experience working in Environment?

Apply today for a rewarding opportunity with the leader in Environment Testing.

This position is full-time, Monday - Friday, 1st shift on site in Yarmouth Maine. Compensation $45,000-50,000 (DOE)

Essential Duties and Responsibilities:

Project Set-up

Project review in LIMS
Sets up project
Adds any project notes (special reporting and invoicing instructions, etc.)
Reviews project documentation
Adds any project documentation to central repository
Sets up client for Total Access
Manages purchase orders, task orders, contracts, and change order requests
Verified that lab compound lists and limits meet project requirements for new projects not quoted
Add any project specific limits/lists to LIMS
Deliverable assignment and delivery route
For new projects not quoted, confirms that EDD format is available (deliverable assignment and delivery route). Submits a helpdesk ticket for any new formats needed.
Communicates project details to operations
Initiates project kick off call with client and pertinent staff, if needed
Engages work share labs, service centers, and non-Eurofins locations as needed for new projects not quoted
Works with operations to ensure adequate capacity for incoming work (forecasting)
Provides updates to operations on upcoming work
Familiarity with state and national program requirements as it pertains to work mix
Create bottle orders
Schedules courier and field sampler, if needed
Confirms non-Eurofins subcontract labs area on the approved list and set-up as vendors for new work
Confirms non-Eurofins subcontract labs are on the approved list and set-up as vendors for existing work
Initiates approval process for any subcontract labs not on the approved list
Generates subcontract paperwork
Generates accounting software requisition when sending subcontract samples
Verifies that lab certification meets project requirements
Verifiers that lab compound lists and limits meet project requirements for new quotes
For new quotes confirms that EDD format is available (delivery assignment and delivery route). If new format is needed, submits a helpdesk ticket
Engages work share labs, service centers, and non-TA locations as needed for new quotes
Provides supporting documentation to client as needed (Contract list, bottle table with preservation, etc)

Sample Receipt

Communicates any issues to clients for duration of project
Manages incoming work for rush and short holds
Reviews log-in
Resolves log-in issues with client
Informs client of any log-in discrepancies
Sets samples to “available” after review
Sends client sample receipt confirmation
Reviews draft invoice
Confirms that any client needed information (Purchase order, project number, etc) is recorded in LIMS for invoicing

Reporting

Client specific report requirements
Reviews job list daily and manages due dates
Communicates any expected delays to clients before the job due date
Confirms any data anomalies (filtered>dissolved, deviations from historicals, etc) with operations before submitting to client
Reviews reports and EDDS before issuing to the client
Confirms correct report format and EDD format is used
Creates and issues final report by client due date
Issues final data packages
State reporting forms and submission
DMR forms
EDD checkers
Data upload
Compiles case narratives

Invoicing

Sets up delivery route
Reviews final invoice before issuing to client
Generates credit/debit memos as needed
Submits credit/debit memos for approval
Submits approved credit/debit memos to client, if needed
Submits revised invoices
Initiates follow up calls to confirm correct invoicing

Works with collections on A/R follow up
Regular review of A/R status

Client Set-up

Work with CSM to communicate lab capabilities to the client
Requests new client review
Confirms sales assignments with Business Development Manager
Takes new quote requests from clients
Reviews client contract requirements/coordinates review
Reviews purchase orders
Submits purchase orders for approval and returns approved orders to client
Follow up on client terms and credit limit

Account Maintenance

Follow up calls and visits with clients
Provides technical support as needed
Uses company resources to follow up on client requests
Familiarity with company capabilities and key contacts
Forward opportunities and leads to sales
Forecasts upcoming work
Asks for the next opportunity
Area of responsibility (air, regulations, etc)
Submits client complaints and participates in correction action/follow up as needed
Communicates client issues/complaints to sales
Follow up on client requests
Supports the follow up of quotes/bids for tracking purposes

Quotes & Proposals

Initiates project QAPP review with operations, QA, and subcontract labs as needed
Initiates technical support from operations as needed (special requests, method development, technical review, etc)
Quote generation and approvals
Reviews client quote requests for capabilities, certifications, scope
Confirms client contracts (if applicable) and pricing
Determines lab placement for the work
Confirms that lab certification meets project requirements
Confirms the lab compound lists and limits meet project requirements
Creates quotes
Submits quotes for approval
Sends quotes to client
Forecasts quotes
Provides QAPP/SOW information to the client as needed
Updates status in LIMS

Qualifications

Minimum Qualifications:

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.

BS/BA in Chemistry/Sciences or related field (four years related experience may substitute for a degree
6-12 months of client relationship/customer service experience
Prefer some bench chemist or field experience
Comfortable with performing some laboratory responsibilities
Requires additional lab training in methods and QA across multiple departments
Working knowledge of environmental regulations
Basic knowledge of the LIMS
Strong interpersonal, communication and problem solving skills
Effective time management
Strong organizational skills
Leadership skills
Multi-tasking
Adaptability and flexibility
Ability to ensure requirements for On-Time Delivery are met
Authorization to work in the United States indefinitely without restriction or sponsorship
Must be able to pass a pre-employment background check and drug screen
Attention to clients: demonstrates a desire to understand customer needs; listens to what customers are saying and asks questions as appropriate; demonstrates awareness of client goals. Follows up with clients during projects and following project completion; keeps clients up to date about decisions that affect them; seeks the comments, criticisms and involvement of clients; adjusts services based on client feedback
Technical familiarity: seeks information from a variety of sources in a variety of ways to respond to client’s technical questions about the project and to effectively communicate project status.
Customer service orientation: strives to meet customer expectations and takes responsibility to resolve client complaints. Provides prompt, efficient and personalized assistance to meet the requirements, requests, and concerns of customers; provides thorough, accurate information to answer customers’ questions and inform them of commitment times or performance guarantees; actively looks for ways to help customers by identifying and proposing appropriate solutions and/or services; establishes boundaries as appropriate for unreasonable customer demands.
Is pleasant, courteous and professional when dealing with internal or external customers; displays a good-natured, cooperative attitude; is calm and empathetic when dealing with hostile customers.
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.

Additional Information

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

Find out more in our career page: https://careers.eurofins.com/

In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.

We do not offer Visa Sponsorship for this role.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Yarmouth, ME, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":8,"item":{"@type":"JobPosting","title":"Laboratory Assistant - Clinical Laboratory","datePosted":"2025-08-13","description":"

Under the general supervision of the Phlebotomy Supervisor and the Laboratory Manager, the Lab Assistant II performs a wide variety of duties in the lab including, but not limited to, specimen collection, specimen processing, data entry, new employee orientation and training, special projects, and general duties.

Providence caregivers are not simply valued – they’re invaluable. Join our team at Queen Of The Valley Medical Ctr and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Required Qualifications:

H.S. Diploma or GED.
California Certified Phlebotomy Technician I License upon hire or California Certified Phlebotomy Technician II License upon hire.
3 years of experience as a Clinical Laboratory Assistant, demonstrating excellence over time.

Why Join Providence?

Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.

\nAt Providence, our strength lies in Our Promise of “Know me, care for me, ease my way.” Working at our family of organizations means that regardless of your role, we’ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable. \n\n

The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.

Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.

Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

","hiringOrganization":{"@type":"Organization","name":"Providence","sameAs":"https://www.providence.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Napa, CA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":9,"item":{"@type":"JobPosting","title":"Medical Laboratory Scientist - Clinical Laboratory","datePosted":"2025-08-06","description":"

Medical Laboratory Scientist

Under the direction of the Section Supervisor, the Medical Technologist employs professional knowledge and judgment to perform technical, physical, clerical and quality assurance functions in the department.

Providence caregivers are not simply valued – they’re invaluable. Join our team at Covenant Children's Hosp (Methodist Children's Hosp) and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Please note the following important details regarding this role:

This role is an onsite position and will report onsite daily as scheduled
Flexibility to work a rotating schedule, including weekends & holidays as scheduled
Work Status Available:
- Per Diem / On Call, Day
- Positions specified as “on call/per diem” refer to employment consisting of shifts scheduled on an “as needed basis” to fill in for staff vacancies.
Shifts Schedule: Sunday-Saturday with various days off. Hours will range from 0500-0700 start time and 1330-1530 end time.

Required Qualifications:

Bachelor's Degree in Medical Technology, Clinical Lab Science or an equivalent science -OR- a combination of equivalent education and work experience

Preferred Qualification:

1 or more years of work experience in a clinical laboratory, preferably in a hospital setting.

Why Join Providence?

Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our mission of caring for everyone, especially the most vulnerable in our communities.

","hiringOrganization":{"@type":"Organization","name":"Providence","sameAs":"https://www.providence.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Lubbock, TX, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":10,"item":{"@type":"JobPosting","title":"Senior Laboratory Assistant/ Laboratory Assistant","datePosted":"2025-08-08","description":"

Senior Laboratory Assistant/ Laboratory Assistant in the School of Clinical Medicine (Ref.: 532823) (to commence as soon as possible, on a two-year fixed-term basis with contract-end gratuity and University contribution to a retirement benefits scheme, totalling up to 10% of basic salary, with the possibility of renewal subject to funding availability and satisfactory performance)

Applicants should possess 5 passes in HKCEE or min. Level 2 (or equivalent) in 5 subjects in HKDSEE, preferably hold a Diploma in Laboratory Sciences or related disciplines. They should have a good command of written and spoken English and Chinese; good organisational and interpersonal skills; a strong sense of responsibility; appropriate IT proficiency; and the ability to work independently and collaboratively within a team. Prior work experience in clinical laboratories and possession of a first aid certificate would have advantages. Those with lower qualifications and/or less experience may be considered for appointment as Laboratory Assistant.

The appointee will support the day-to-day operation of a clinical laboratory and maintenance of facilities, including the preparation of apparatus for laboratory teaching activities, operation of electronic devices, data entry and record keeping, procurement of equipment, and other duties as assigned. He/She will also assist in the setting up of a state-of-the-art simulation training centre for medical students. Shortlisted candidates will be invited to attend an interview.

A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.

The University only accepts online application for the above post. Applicants should apply online and upload an up-to-date C.V. Review of applications will start from August 21, 2025 and continue until August 31, 2025, or until the post is filled, whichever is earlier.

","hiringOrganization":{"@type":"Organization","name":"The University of Hong Kong","sameAs":"https://www.hku.hk/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hong Kong","addressCountry":"Hong Kong","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":11,"item":{"@type":"JobPosting","title":"Laboratory Director, A & L Laboratory","datePosted":"2025-08-15","description":"

Company Description

Job Description

This fast-paced laboratory conducts a variety of analysis ranging from wet chemistry, Ion Chromatography, microbiological and radiological testing of drinking water. A & L Laboratory- A Division of Granite State Analytical. Must live a commutable distance to Auburn, Maine

Compensation range: $70,000- $85,000 (DOE) Must live a commutable distance to Auburn, Maine

The Laboratory Director is responsible for maintaining positive operating margin at the laboratory level and for meeting and exceeding the annual budget. Supervises all laboratory personnel and provides leadership and direction as needed. Responsible for ensuring compliance and integration of facility operation with corporate and regulatory policies and procedures. The lab director will serve as a liason with corporate business partners and will champion Company policies, vision, and mission.

Essential Duties and Responsibilities:

Manages the laboratory to provide positive operating margin and meet annual budgetary goals.
Growing the organization's lab service offerings to meet organizational strategic objectives.
Working with all laboratories' operations to continuously improve lab technical capabilities and services.
Developing and validating methods, work instructions, and training for all laboratory employees.
Ensure laboratory operations meet the technical quality objectives required by various accrediting bodies.
Assists with data entry, quality control, and sample receipt as needed.
Develop and implement laboratory policies and procedures to ensure compliance with industry standards.
Provide technical guidance, consultation and support to laboratory staff.
Provide scientific and technical leadership to laboratory staff and support their professional growth and development.
The laboratory director will be responsible for the culture of the lab and the employee engagement of personnel under their hierarchy. The lab director will act confidentially in employee matters and partner with Human Resources to ensure that all policies and programs are applied consistently throughout the laboratory.
Builds and maintains positive customer relationships and sales growth through direct interaction with customers and Eurofins Environment Testing America sales personnel.
Establishes and maintains an active and positive safety culture and ensures that the Employee Health and Safety procedures are implemented and followed to maintain facility operations that are compliant with appropriate policies and regulations.
Collaborates with the Quality Assurance Manager to ensure that standard operating procedures for the facility are implemented and reviewed on a regular basis so that the facility is operated in a compliant manner which allows it to produce defensible data.
Prioritizes the activities of the operations groups to ensure key goals are achieved and customer service needs are addressed. Provides periodic reports to ensure that goals and objectives are being achieved and to recognize opportunities for development.
Works with Project Managers and Customer Service Managers to ensure the accurate forecast of receipts, provide quality analytical data to clients and meet on- time delivery dates.
Communicates facility-specific goals and objectives to employees. Communicates and implements company initiatives designed to foster teamwork and communication.
Fulfills supervisory responsibilities with direct reports to achieve strong staff performance. Mentors key employees.
Evaluates and maintains appropriate staffing levels to support operational needs and budgetary requirements. Collaborates with the Business Controller and HR Business Partner to discuss and review manpower regularly
Actively participates in the process of sharing and adopting best practices within Eurofins Environment Testing America. Provides technical assistance to other Eurofins Environment Testing America laboratories as needed to improve productivity and customer service.
Responsible for upholding and enforcing Company policies, including but not limited to, Quality, Safety, Standard Operating Procedures, Ethics, and Harassment.
Expected to champion Health & Safety and assume ownership for the safety of those employees within her/his responsibility

Qualifications

Basic Minimum Qualifications (BMQ)

Education/Experience-

BS in Chemistry or a science-related field required with at least 30 college semester credit hours in chemistry.
5 years management experience
5 years analytical experience or related technical knowledge preferred

Ability and/or Skills-

Familiarity with laboratory operations and services

Familiarity with EPA, DOT, OSHA, and DOL regulations
Excellent verbal and written skills  Strong customer relations skills
Ability to manage a business at a profit/loss responsibility level
Ability to control operating budgets
Ability to develop and enforce policies and operating practices
Ability to prioritize and delegate responsibilities
Ability to successfully handle contract and other negotiations
Strong decision-making abilities
Problem-solving abilities

Disclaimer: This position description is written as a guideline to inform employees of what is generally expected of them at each job level. The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment. Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole. The above information may not be used or duplicated by others without written consent.

Additional Information

Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

Find out more in our career page: https://careers.eurofins.com/

In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.

We do not offer Visa Sponsorship for this role.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Auburn, ME, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":12,"item":{"@type":"JobPosting","title":"Supervisor Clinical Laboratory - Clinical Laboratory","datePosted":"2025-08-19","description":"

Supervisor Clinical Laboratory - Clinical Laboratory at Providence St. Joseph Medical Center in Burbank, CA. This position is Full-time and will work evening shifts.

Providence St. Joseph Medical Center is proud to be Magnet® recognized, the nation’s highest recognition for nursing excellence. The American Nurses Credentialing Center’s Magnet Recognition Program® recognized the hospital’s nursing team for exemplary patient care, nursing practice collaboration, patient outcomes and nursing research. In addition, Providence St. Joseph is recognized as one of the best regional hospitals in 11 types of care by U.S. News & World Report.

The Pathology Supervisor is responsible for daily operations, personnel management and technical expertise of the Anatomic laboratory section. Performs all duties in a manner which promotes team concept and reflects the mission philosophy of the Providence Health System. Provides technical oversight of department as well as ensuring accurate, timely and cost effective service for all laboratory customers. Responsible for all regulatory requirements as required by CLIA 88, CAP and the Joint Commission.

Providence caregivers are not simply valued – they’re invaluable. Join our team at St Joseph Medical Center and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Required Qualifications:

Completion of education and training as a Histologist (HT-ASCP) or Cytologist (CT-ASCP).
National Certification from American Society for Clinical Pathology upon hire or
California Clinical Laboratory Scientist License California upon hire or
California Clinical Chemist Scientist License upon hire or
California Clinical Immunohematologist Scientist License upon hire or
California Clinical Microbiologist Scientist License upon hire or
California Clinical Toxicologist Scientist License upon hire or
California Clinical Cytogeneticist Scientist License upon hire or
California Clinical Genetic Molecular Biologist Scientist License upon hire or
California Clinical Hematology Scientist License upon hire or
California Clinical Histocompatibility Scientist License upon hire or
California Clinical Laboratory Scientist Biochemistry Special License upon hire or
California Certified Phlebotomy Technician I License upon hire or
California Certified Phlebotomy Technician II License upon hire or
National Certification from American Society for Clinical Pathology upon hire.

Preferred Qualifications:

Bachelor's Degree
5 years of work experience in pathology.
Previous supervisory experience

Why Join Providence?

","hiringOrganization":{"@type":"Organization","name":"Providence","sameAs":"https://www.providence.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Burbank, CA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":13,"item":{"@type":"JobPosting","title":"Analyst II/Project Manager- Environmental Testing Laboratory-Eurofins Environment Testing","datePosted":"2025-08-19","description":"

Company Description

Job Description

Eurofins Environment Testing is searching for a Project Manager with Lab Responsibilities. 60/40 split on time. This position is on location in Portland, Maine and candidates should live within a commutable distance to the lab.

Do you have 5 years of Project Management experience working in Environment?

Do you have experience in wastewater and drinking water?

Biochemical Oxygen Demand?

IDEXX microbiology methods (Colilert, Enterolert, Legiolert, HPC)?

If you have met these requirements- Please apply today for a rewarding opportunity with the leader in Environment Testing.

This position is full-time, Monday - Friday, 1st shift. Compensation $45,000-50,000+ (DOE)

Essential Duties and Responsibilities for Analyst II:

Performs laboratory procedures requiring knowledge of scientific methods and testing procedures including:
- Batching and prepping samples for analysis taking into account special and varied client and quality assurance requirements
- Making reagents for sample analysis
- Aliquots extracted samples to maximize laboratory productivity
- Preparing appropriate standards to ensure compliant data
- Determining appropriate routine and complex analysis methods for a wide variety of organic and inorganic samples
- Operation, calibration, and maintenance of laboratory instruments
Upload data into LIMS system for review.

Essential Duties and Responsibilities for Project Manager:

Project Set-up

Project review in LIMS
Sets up project
Adds any project notes (special reporting and invoicing instructions, etc.)
Reviews project documentation
Adds any project documentation to central repository
Sets up client for Total Access
Manages purchase orders, task orders, contracts, and change order requests
Verified that lab compound lists and limits meet project requirements for new projects not quoted
Add any project specific limits/lists to LIMS
Deliverable assignment and delivery route
For new projects not quoted, confirms that EDD format is available (deliverable assignment and delivery route). Submits a helpdesk ticket for any new formats needed.
Communicates project details to operations
Initiates project kick off call with client and pertinent staff, if needed
Engages work share labs, service centers, and non-Eurofins locations as needed for new projects not quoted
Works with operations to ensure adequate capacity for incoming work (forecasting)
Provides updates to operations on upcoming work
Familiarity with state and national program requirements as it pertains to work mix
Create bottle orders
Schedules courier and field sampler, if needed
Confirms non-Eurofins subcontract labs area on the approved list and set-up as vendors for new work
Confirms non-Eurofins subcontract labs are on the approved list and set-up as vendors for existing work
Initiates approval process for any subcontract labs not on the approved list
Generates subcontract paperwork
Generates accounting software requisition when sending subcontract samples
Verifies that lab certification meets project requirements
Verifiers that lab compound lists and limits meet project requirements for new quotes
For new quotes confirms that EDD format is available (delivery assignment and delivery route). If new format is needed, submits a helpdesk ticket
Engages work share labs, service centers, and non-TA locations as needed for new quotes
Provides supporting documentation to client as needed (Contract list, bottle table with preservation, etc)

Sample Receipt

Communicates any issues to clients for duration of project
Manages incoming work for rush and short holds
Reviews log-in
Resolves log-in issues with client
Informs client of any log-in discrepancies
Sets samples to “available” after review
Sends client sample receipt confirmation
Reviews draft invoice
Confirms that any client needed information (Purchase order, project number, etc) is recorded in LIMS for invoicing

Reporting

Client specific report requirements
Reviews job list daily and manages due dates
Communicates any expected delays to clients before the job due date
Confirms any data anomalies (filtered>dissolved, deviations from historicals, etc) with operations before submitting to client
Reviews reports and EDDS before issuing to the client
Confirms correct report format and EDD format is used
Creates and issues final report by client due date
Issues final data packages
State reporting forms and submission
DMR forms
EDD checkers
Data upload
Compiles case narratives

Invoicing

Sets up delivery route
Reviews final invoice before issuing to client
Generates credit/debit memos as needed
Submits credit/debit memos for approval
Submits approved credit/debit memos to client, if needed
Submits revised invoices
Initiates follow up calls to confirm correct invoicing

Works with collections on A/R follow up
Regular review of A/R status

Client Set-up

Work with CSM to communicate lab capabilities to the client
Requests new client review
Confirms sales assignments with Business Development Manager
Takes new quote requests from clients
Reviews client contract requirements/coordinates review
Reviews purchase orders
Submits purchase orders for approval and returns approved orders to client
Follow up on client terms and credit limit

Account Maintenance

Follow up calls and visits with clients
Provides technical support as needed
Uses company resources to follow up on client requests
Familiarity with company capabilities and key contacts
Forward opportunities and leads to sales
Forecasts upcoming work
Asks for the next opportunity
Area of responsibility (air, regulations, etc)
Submits client complaints and participates in correction action/follow up as needed
Communicates client issues/complaints to sales
Follow up on client requests
Supports the follow up of quotes/bids for tracking purposes

Quotes & Proposals

Initiates project QAPP review with operations, QA, and subcontract labs as needed
Initiates technical support from operations as needed (special requests, method development, technical review, etc)
Quote generation and approvals
Reviews client quote requests for capabilities, certifications, scope
Confirms client contracts (if applicable) and pricing
Determines lab placement for the work
Confirms that lab certification meets project requirements
Confirms the lab compound lists and limits meet project requirements
Creates quotes
Submits quotes for approval
Sends quotes to client
Forecasts quotes
Provides QAPP/SOW information to the client as needed
Updates status in LIMS

Qualifications

Minimum Qualifications:

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required.

BS/BA in Chemistry or related field (3 years laboratory experience may substitute for a degree)
Minimum 2 years experience in routine and complex laboratory procedures and instruments, preferably in a production environment.
6-12 months of client relationship/customer service experience
Prefer some bench chemist or field experience
Comfortable with performing some laboratory responsibilities
Requires additional lab training in methods and QA across multiple departments
Working knowledge of environmental regulations
Basic knowledge of the LIMS
Strong interpersonal, communication and problem solving skills
Effective time management
Strong organizational skills
Leadership skills
Multi-tasking
Adaptability and flexibility
Ability to ensure requirements for On-Time Delivery are met
Authorization to work in the United States indefinitely without restriction or sponsorship
Must be able to pass a pre-employment background check and drug screen
Attention to clients: demonstrates a desire to understand customer needs; listens to what customers are saying and asks questions as appropriate; demonstrates awareness of client goals. Follows up with clients during projects and following project completion; keeps clients up to date about decisions that affect them; seeks the comments, criticisms and involvement of clients; adjusts services based on client feedback
Technical familiarity: seeks information from a variety of sources in a variety of ways to respond to client’s technical questions about the project and to effectively communicate project status.
Customer service orientation: strives to meet customer expectations and takes responsibility to resolve client complaints. Provides prompt, efficient and personalized assistance to meet the requirements, requests, and concerns of customers; provides thorough, accurate information to answer customers’ questions and inform them of commitment times or performance guarantees; actively looks for ways to help customers by identifying and proposing appropriate solutions and/or services; establishes boundaries as appropriate for unreasonable customer demands.
Is pleasant, courteous and professional when dealing with internal or external customers; displays a good-natured, cooperative attitude; is calm and empathetic when dealing with hostile customers.
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.

Additional Information

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

Find out more in our career page: https://careers.eurofins.com/

In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.

We do not offer Visa Sponsorship for this role.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Portland, ME, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":14,"item":{"@type":"JobPosting","title":"Project Manager/Senior Project Manager","datePosted":"2025-08-08","description":"

Electrical Consultants, Inc. (ECI), a leading power engineering consultant firm, is seeking a motivated individual to join our Denver, CO office (physically located in Centennial, CO) as a Project manager or Senior Project Manager. The successful candidate will be responsible for performing electrical and physical drafting and design work for electrical substations ranging from 4 kV to 500 kV.

Responsibilities include assuming responsibility for programs and projects as well as development of engineering standards and business tools to improve efficiencies and enhance the reputation of ECI. Assume a high level of contribution in executing ECI's work development plans and goals under the direction of the Executives, Senior/General Managers. Represent and in the best interests of ECI and make decisions and recommendations that are authoritative and have an important impact on the health and vitality of ECI. Oversee and manage the successful execution of High Voltage Substation projects with duties including - but not limited to:

Oversee and coordinate activities of multidisciplinary teams to ensure projects are executed in accordance with approved scope, budget and schedule.
Interface with internal and external clients - including project managers, SME engineering individuals and teams, commercial personnel and officers of other organizations.
Demonstrate a high degree of creative, foresight and mature judgment in planning, organizing, and guiding extensive and detailed engineering activities.

Minimum Requirements: BSEE or BSCE and 14 years' experience, or a M.S. degree in engineering with sufficient experience required for advancement as determined by management, or a combination of applicable education and experience as determined by management; professional registration (engineer or surveyor); demonstrated capability to effectively perform project management for large size engineering projects in a hands-on manner. The successful applicant must have proven effective verbal and written communication skills, proven excellent level of interpersonal skills, and ability to work individually and on a team. Must be detail oriented and possess a high level of organizational skills. Must possess a proven ability to work with confidential information and proven ability to exercise independent judgment. The successful applicant may be subject to client mandated drug and background checking. Occasional travel/driving will be required. Successful applicant is subject to ECI's auto insurance carrier requirements. Applicants must not require sponsorship for employment visa status (e.g., H-1B visa status) now or in the future.

Salary commensurate with experience and education. Benefits package includes:

Medical, dental and vision insurance
Flexible spending account
Health savings account
Life insurance
Disability insurance
401(k), profit sharing and employee stock ownership plan
Paid vacation, personal days and holidays
Paid Parental Leave
Continued professional education reimbursement

Electrical Consultants, Inc. (ECI) employs over 850 engineers, designers, project managers, surveyors, ROW agents, environmental planners, construction professionals and support staff in 37 offices across the U.S. The firm has more than 40 years of experience in the planning, engineering, and construction of a wide range of power delivery projects including substations, transmission lines, distribution systems, communication systems and industrial facilities. Visit our website at www.eciusa.com.

An Equal Opportunity Employer

","hiringOrganization":{"@type":"Organization","name":"Electrical Consultants, Inc.","sameAs":"https://eciusa.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Centennial, CO 80122, US","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":15,"item":{"@type":"JobPosting","title":"Project Manager/Senior Project Manager","datePosted":"2025-08-04","description":"

Company Description

Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries.
\nWorking with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve people’s lives. Working in partnership makes it possible to deliver the world’s most impactful projects and programmes as we turn challenge into opportunity and complexity into success.
\nOur capabilities include programme, project, cost, asset and commercial management, controls and performance, procurement and supply chain, net zero and digital solutions.
\nWe are majority-owned by CBRE Group, Inc., the world’s largest commercial real estate services and investment firm, with our partners holding a significant minority interest. Turner & Townsend and CBRE work together to provide clients with the premier programme, project and cost management offering in markets around the world.
\nPlease visit our website: www.turnerandtownsend.com

Job Description

Preparation of procurement documentation and subsequent procurement activities, including Head Contractor and Managing Contractor Contract.
Preparation of Public Works Committee documentation.
Design Management and Coordination.
Extensive Stakeholder Consultation/Management
Manage/lead multiple project commitments
Lead, chair and minute client meetings / discussions
Work with team lead to pursue business initiatives
Commission Management (SPM roles)

Qualifications

A recognised Degree or equivalent qualification relating to a technical field: Construction Management or Project Management, Engineering, Architecture, Cost Management or relatable trade experience
5 + years project management experience (ideally client side/consulting)
Baseline clearance preferred
Ability to thrive in a high pressure, fast paced environment.
Advanced Microsoft skills are essential and Primavera skills will be highly regarded
Technical ability to lead and manage complex projects and programs as the key client interface
Excellent command of written and spoken English with excellent report and bid writing skills.
Strong leadership skills with the ability to lead and develop a team
Highly motivated and driven with a passion for delivering to your client

Additional Information

Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change.

We want our people to succeed both in work and life. To support this we promote a healthy, productive, and flexible working environment that respects work-life balance. 

At Turner & Townsend we firmly believe that our people are at the heart of our success and we continually strive to create a great place to work.

We promote integrity in everything that we do and apply our expertise to shape a better environment for future generations and, ultimately, generate value for our communities.

Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from Aboriginal and Torres Strait Islanders and people from all sectors of the community. 

Turner & Townsend does not accept any speculative or unsolicited CV’s that have been sent to our internal recruitment team or hiring managers from agencies outside of our preferred supplier list. Any speculative or unsolicited CV’s will be treated as a direct application.

Please find out more about us at www.turnerandtownsend.com/

#LI-LN2

Join our social media conversations for more information about Turner & Townsend and our exciting future projects:

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It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time.

Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review.

","hiringOrganization":{"@type":"Organization","name":"Turner & Townsend","sameAs":"https://www.turnerandtownsend.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Canberra, ACT, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":16,"item":{"@type":"JobPosting","title":"Senior Project Manager/Project Manager","datePosted":"2025-08-18","description":"

Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets.

We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world’s most complex challenges and deliver more impact together.

Role description:

Arcadis is seeking an experienced Senior Project Engineer / Project Manager to join our Resilience Water team in Middletown, CT to support our growing portfolio of water and wastewater infrastructure planning, design and construction projects. In this role, you will lead and support accounts and project teams to deliver water and wastewater conveyance/treatment design & construction engineering projects. You will be a critical member of our team and be expected to support the proven reputation of excellence in Client Management/Development along with executing and managing projects.

Role accountabilities:

This role supports projects and clients in the planning, preliminary and final design, and construction of water/wastewater treatment plants, collection systems, pump/lift stations, drainage improvements, as well as creating construction documents, specifications, and providing engineering services during construction.

Leadership: Function as an account lead and project manager as part of a delivery team. This will entail ensuring technical leadership and quality control is in place for diverse, multidisciplinary delivery teams throughout all phases of a project.

Client Liaison: Functioning as the primary interface between the client staff and the consultant team. You will engage with the client regularly from a position of familiarity with the consultant team’s advances and actively participate in knowledge sharing, brainstorming, and work planning with client staff. Part of this responsibility will be to manage existing and an expanding base of clients by meeting or exceeding their expectations, by delivering quality work, and through active communication.

Project Management: Function as the project manager in establishing meeting project schedules, budgets, and quality objectives; assigning and monitoring of tasks; and ensuring adequate resources to deliver the work. The ideal candidate must be able to work on a variety of projects simultaneously, as well as providing technical expertise and experience on other related projects. You will lead detailed engineering calculations and analysis as well as prepare cost estimates, project documentation and ensure design tasks are within budget and on schedule

Miscellaneous: Mentor junior-level technical staff and travel as needed for client meetings, project site visits, etc. (25%)

Key Skills and Attributes:

The ideal candidate will possess strong leadership skills including experience managing project delivery, prioritizing tasks, coordinating with design disciplines, and overseeing project budgets and schedules. They should have a solid background in the design and construction of municipal water and wastewater treatment facilities, collection systems, and pump stations, with a focus on expansion, rehabilitation, and retrofits. Flexibility to collaborate with various project teams locally and across remote offices is essential. Additionally, the candidate should have experience in developing project drawings, technical specifications, schedules, and cost estimates. Strong client-facing skills are also required including the ability to prepare and develop proposals, manage client expectations, and foster positive client relationships.

Qualifications & Experience:

Required Qualifications:

Bachelor’s Degree in Civil or Environmental Engineering or related field, Master’s preferred.
Professional Engineering Licensure in Massachusetts and/or in other nearby states
Minimum of 10 years of related industry experience in the water/wastewater field

Preferred Qualifications

Active participation in regional (local/state) and/or national professional associations
Experience mentoring and developing project teams and staff

Why Arcadis?

We can only achieve our goals when everyone is empowered to be their best. We believe everyone's contribution matters. It’s why we are pioneering a skills-based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together.

You’ll do meaningful work, and no matter what role, you’ll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark, on your career, your colleagues, your clients, your life and the world around you.

Together, we can create a lasting legacy.

Join Arcadis. Create a Legacy.

Our Commitment to Equality, Diversity, Inclusion & Belonging

We want you to be able to bring your best self to work every day which is why we take equality and inclusion seriously and hold ourselves to account for our actions. Our ambition is to be an employer of choice and provide a great place to work for all our people. We are an equal opportunity and affirmative action employer. Women, minorities, people with disabilities and veterans are strongly encouraged to apply. We are dedicated to a policy of non-discrimination in employment on any basis including race, creed, color, religion, national origin, sex, age, disability, marital status, sexual orientation, gender identity, citizenship status, disability, veteran status, or any other basis prohibited by law.

Arcadis offers benefits for full time and part time positions. These benefits include medical, dental, and vision, EAP, 401K, STD, LTD, AD&D, life insurance, paid parental leave, reward & recognition program and optional benefits including wellbeing benefits, adoption assistance and tuition reimbursement. We offer nine paid holidays and 15-20 days PTO that accrue per year. The salary range for this position is $110,000 - $175,000. Actual salaries will vary and are based on several factors, such as experience, education, budget, internal equity, project and location.

#Resilience-ANA
#Water-ANA

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Company Description

School of Engineering and Digital Sciences, Nazarbayev University

Job Description

Laboratory assistant performs the following duties and responsibilities:

1) collaborates with the Faculty and Teaching Assistants of the School in the preparation of laboratory sessions;

2) prepares necessary consumables and equipment for laboratory sessions;

3) conducts modeling of laboratory sessions together with Teaching Assistants;

4) conducts regular visits of the laboratories;

5) performs activities related to the installation, maintenance, configuration, and ongoing testing of laboratory equipment;

6) maintains laboratory equipment in good working condition, if necessary, with the assistance of the Office of the Provost - Engineering and Technical Services;

7) conducts an inventory of laboratory equipment and consumables regularly;

8) determines the need for protective equipment and other necessary supplies for laboratories in conjunction with the Health and Safety Department (hereinafter referred to as HSD);

9) conducts instructions in the laboratory for students/laboratory users, within the framework of his/her official duties and powers;

10) develops standard operating procedures (SOP) for equipment and health and safety instructions for potentially dangerous types of work in conjunction with the HSD;

11) conducts training sessions on the use of equipment for persons assigned to work in the laboratory;

12) assists in preparing the budget requests for the relevant reporting period, including preparation of justifications;

13) prepares technical specifications for procurement of goods together with the initiator;

14) participates in acceptance, verification, testing of the purchased equipment and consumables for the laboratory as a member of the acceptance committee;

15) participates in the annual inventory of fixed assets of the School together with concerned structural divisions of the University;

16) prepares documents for writing off the necessary consumables from the University's warehouses;

17) provides reports, information, and data at the request of the structural divisions and organizations of the University, in agreement with the School's management, within the competence;

18) ensures the safety of documents within the framework of supervised direction;

19) maintains correspondence within the scope of his/her functional responsibilities;

20) participates in the identification, evaluation, management, and monitoring of risks within the framework of supervised direction;

21) temporarily performs the duties (replaces) of the other Laboratory assistant during his/her temporary absence (up to one month);

22) timely and properly executes the tasks of the line manager and the University`s management;

23) observes the requirements of the legislation of the Republic of Kazakhstan and the Employer`s internal documents;

24) is responsible for exercising the labor and performance discipline;

25) is responsible for ensuring the integrity of official documents, and prevention of the disclosure or leakage of confidential and business information, as well as information of restricted access by the legislation, Charter, and internal documents of the Employer;

26) in case of dismissal, is responsible for the timely transfer of all paper documentation, digital information, inventory to another employee as instructed by the line manager (to be certified by the act of acceptance-transfer).

Qualifications

Education

Higher-professional, preferable from the higher education institutions with the English language of instruction;

Priority specializations:

- Engineering and Technical;

- Chemistry and Technologies;

- Engineering and Construction;

- Computer science

Work experience

One year minimum. No working experience with a master`s degree in the relevant area

Knowledge

- Knowledge in the relevant field: Engineering and technical/Chemical-technological/Engineering-construction/Computer science;

- knowledge of the basic principles of preparing a technical specification for equipment or consumables;

- knowledge of safety regulations when working in the laboratory;

- knowledge of MS Office, Excel, PowerPoint programs;

- fluent in English, Kazakh, and Russian languages.

Skills

- Skills in preparing and conducting presentations;

- skills in working with basic laboratory equipment

Other requirements

- Commitment to the goals and values of the University;

- ability to work independently, as well as part of a team;

- sociability;

- responsibility;

- initiative;

- responsible approach to work

Additional Information

Recruitment and selection process
Recruitment and selection at Nazarbayev University include the following process: preliminary selection based on experience and qualifications, assessments (e.g. technical skills/capabilities, aptitude, personality, work samples, in-basket exercises, and informal interviews), and motivation.

Formal interviews form the final stage of the selection process.
They are typically based on organizational values and behaviors and conducted in English.
You are encouraged to share your views and values to identify how they fit into Nazarbayev University core values

","hiringOrganization":{"@type":"Organization","name":"Nazarbayev University","sameAs":"https://nu.edu.kz"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Astana, ASTANA, Kazakhstan","addressCountry":"Kazakhstan","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":18,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-07-18","description":"

Park Nicollet is looking to hire a Laboratory Assistant to join our team! Come join us as a Partner for Good and help us make an impact on the care and experience that our patients and their families receive every day.

Position Summary: The Laboratory Assistant will provide a wide range of laboratory services including specimen collection, client service and reception desk duties, ordering/ scheduling/ billing functions, laboratory testing, phlebotomy, dispatching, specimen processing, centrifuging, delivery of specimens to appropriate laboratory/department and assuring proper efficiency and workflow management. Position will also serve as a resource for questions from hospital and clinic staff regarding specimen handling and processing.

Required Qualifications:

Strong customer service skills.
Ability to work independently.
Good problem-solving skills.
Demonstrates knowledge of age-related growth and development principles necessary to provide appropriate service and assure safety of patients.
Demonstrates strong organizational skills with the ability to meet time sensitive customer requests and changes on short notice.
If travel is required for the position, team member must have a valid driver’s license and meet the insurability requirements relating to Park Nicollet’s motor vehicle violation criteria.

Preferred Qualifications:

High school graduate or equivalent.
Experience in a medical related field or an applied science degree.
Certification in phlebotomy and one year hospital experience. ASCP certification for phlebotomy is preferred.

Benefits:

Park Nicollet offers a competitive benefits package (for eligible positions) that includes medical insurance, dental insurance, a retirement program, time away from work, insurance options, tuition reimbursement, an employee assistance program, onsite clinic and much more!

At HealthPartners we believe in the power of good – good deeds and good people working together. As part of our team, you’ll find an inclusive environment that encourages new ways of thinking, celebrates differences, and recognizes hard work.

We’re a nonprofit, integrated health care organization, providing health insurance in six states and high-quality care at more than 90 locations, including hospitals and clinics in Minnesota and Wisconsin. We bring together research and education through HealthPartners Institute, training medical professionals across the region and conducting innovative research that improve lives around the world.

At HealthPartners, everyone is welcome, included and valued. We’re working together to increase diversity and inclusion in our workplace, advance health equity in care and coverage, and partner with the community as advocates for change.

Benefits Designed to Support Your Total Health
As a HealthPartners colleague, we’re committed to nurturing your diverse talents, valuing your dedication, and supporting your work-life balance. We offer a comprehensive range of benefits to support every aspect of your life, including health, time off, retirement planning, and continuous learning opportunities. Our goal is to help you thrive physically, mentally, emotionally, and financially, so you can continue delivering exceptional care.

Join us in our mission to improve the health and well-being of our patients, members, and communities.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant because of race, color, sex, age, national origin, religion, sexual orientation, gender identify, status as a veteran and basis of disability or any other federal, state or local protected class.

","hiringOrganization":{"@type":"Organization","name":"HealthPartners","sameAs":"https://www.healthpartners.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Saint Louis Park, MN, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":19,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-07-18","description":"

*** This is a Temporary Position from 9/01/2025 to 8/31/2026 ***

Job Summary: The Laboratory Assistant performs operational level work in a teaching or research lab requiring delicate manual and/or manipulative skills in a limited variety of tasks where a thorough understanding of the principals are not involved. Performs other duties as needed.

Education and Experience: Minimum one year of laboratory experience preferred.

Knowledge and Skills: Able to read; write legibly; speak in English with professional quality; use computer, printer, and software programs necessary to the position (e.g., Word, Excel, Outlook, and PowerPoint). Operate and troubleshoot basic office equipment required for the position; Able to relate and communicate positively, effectively, and professionally with others; work calmly and respond courteously when under pressure; collaborate and accept direction. Able to communicate effectively on the telephone; manage multiple assignments effectively; organize and prioritize workload; work well under pressure; problem solve; pay close attention to detail; work independently with minimal supervision. Able to distinguish colors as necessary; hear sufficiently for general conversation in person and on the telephone, and identify and distinguish various sounds associated with the workplace; see adequately to read computer screens, and written documents necessary to the position.

Licensures and Certifications: None

\nOur mission is to continue the teaching and healing ministry of Jesus Christ. Our core values are compassion, excellence, humility, integrity, justice, teamwork and wholeness.","hiringOrganization":{"@type":"Organization","name":"Loma Linda University Health","sameAs":"https://lluh.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Loma Linda, CA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":20,"item":{"@type":"JobPosting","title":"Laboratory Aide","datePosted":"2025-07-18","description":"

Job Description

Registers patient; and accepts, verifies, logs, examines, sorts, aliquots, prepares and distribute/stores specimens in accordance with established protocols and procedures. Enters or reports lab results per procedures. Maintains operating supply levels and work areas. Performs phlebotomy, as needed.

Job Responsibility

* Registers patients following proper coding procedures.
* Receives orders in the Laboratory Information System.
* Verifies collection lists.
* Logs test orders.
* Uses centrifuge to spin down appropriate tubes.
* Examines specimens for unacceptability and takes appropriate actions. Documents necessary information.
* Separates and aliquots blood and urine specimens, as needed Places tubes not requiring aliquoting into appropriate racks.
* Processes specimens to prepare for testing and resulting.
* Measures 24-hour urine tests, records volumes and aliquots for ordered tests.
* Generates labels via Laboratory Information Systems.
* Delivers specimens to appropriate areas.
* Draws blood from patients.
* Maintains proper levels of supplies.
* Enters reference lab results.
* Notifies physician (or appropriate personnel) of critical values and documents notification.
* Maintains cleanliness of work area and follows established safety and infection control procedures. \\
* May transport specimens, reports or supplies between various offsite locations.
Performs related duties as required.

*ADA Essential Functions

PHYSICAL DEMANDS:

Frequent sitting, bending, standing, walking, carrying of small objects. Occasional pushing, stooping, stretching, pulling, lifting (objects 5 to 10 lbs)

Job Qualification

High School Diploma or equivalent, required.
Minimum of one (1) year related experience including Phlebotomy skills and Laboratory procedures.
Performing blood draws for homebound patients*
No Holidays*

*Additional Salary Detail
The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

","hiringOrganization":{"@type":"Organization","name":"Northwell Health","sameAs":"https://www.northwell.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Staten Island, Richmond, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":21,"item":{"@type":"JobPosting","title":"Laboratory Supervisor","datePosted":"2025-06-30","description":"

Lab Supervisor

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

As a Lab Supervisor you will lead a team of 6 analysts. You will oversee the in process testing, lab operations.

A Typical Day in this role will include;

Manage laboratory personnel and operations within approved budget.
Create and maintain a high-performance collaborative Laboratory team with focus on customer needs, compliance and efficient operation.
Lead and demonstrate expertise in the areas of Chemistry and Microbiology in-line with Quality System requirements, ISO standards and corporate requirements.
Drive continuous improvement initiatives to improve Lab Efficiencies.
Ensure that all testing and operational procedures and practices comply with current regulatory requirements and corporate standards.
Adopt new products to the site into the laboratory testing schedule through change control and validations in accordance with applicable regulations.
Interpret analytical results and work with AS&T to resolve technical and/or operational problems; and provide technical advice and support to other departments within the facility.
Keep up to date with technical and regulatory trends and ensure laboratory operations reflect same and are maintained in validated state.
Utilize LEAN methodologies to achieve improved efficiencies in the laboratory.
Back up and support analytical data review in the laboratory
Ensure Analysts in the Lab are cross trained across Chemistry and Microbiology.
Ensure Lab equipment performance is maintained by preventative maintenance of lab equipment and adequate Laboratory systems.
Adhere to inhouse Health and Safety requirements.
Ensure continual Quality System compliance by adherence to regulations and Alcon requirements.
Participate in the annual Lab budget preparation and monitor budget expenditure.

What you’ll bring to Alcon:

Bachelors degree in chemistry or pharmacy with experience in Pharma or medical device
Minimum 2 years experience in people management.
Must have good PC skills.
Detail orientated and organized.
Good multitasking ability.
Positive attitude & Team player.

How You Can Thrive At Alcon

A competitive salary package with fixed salary, bonus, pension and health insurance
A flexible work environment with competent and committed colleagues. We enjoy working together in a good and respectful manner, and we celebrate our common successes
See your career like never before with focused growth and development opportunities

Alcon Careers

See your impact at www.alcon.com/career

ATTENTION: Current Alcon Employee/Contingent Worker

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","hiringOrganization":{"@type":"Organization","name":"Alcon","sameAs":"https://www.alcon.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Cork, Ireland","addressCountry":"Ireland","addressRegion":"Europe"}}}},{"@type":"ListItem","position":22,"item":{"@type":"JobPosting","title":"Laboratory Scientist","datePosted":"2025-07-21","description":"Summary:\nSupport and/or development and validation of methods to test new products manufactured at the site. Design testing of experimental, confirmation and registration lots, stabilities and new supplier certifications. Participate and/or develop the transfer of analytical technology to the commercial laboratories. \n \nPrimary Functions:\n\n<ol>\n\t<li>Designs experiments to generate analytical methods suitable to support formulation development.</li>\n\t<li>Develops and validates cleaning and analytical methods.</li>\n\t<li>Performs compendial methods evaluation and prepares verification protocols and reports.</li>\n\t<li>Evaluates the data generated by laboratory technologist and or laboratory analysts and trends.</li>\n\t<li>Assures all the information regarding to the testing activities is documented on a timely manner in the corresponding laboratory logbooks and laboratory notebooks.</li>\n\t<li>Prepares API, Raw Materials and Finished Product Specifications and Analytical Methods.</li>\n\t<li>Evaluates Technical Transfer Packages and prepares Analytical Method Transfer Protocols and Reports. Evaluates raw data, perform troubleshooting of analytical methods and oversee laboratory work performed by laboratory analyst and technologists.</li>\n\t<li>Performs or supports laboratory investigations as required.</li>\n\t<li>Prepares progress reports and participate in Staff Meetings.</li>\n\t<li> Acts as a backup contact for the Analytical Development Manager.</li>\n\t<li>Revises SOPs and keeps track of the weekly schedule.</li>\n\t<li>Provides training to laboratory analyst and laboratory technologist as need.</li>\n\t<li>Assures that files and records are maintained up to date.</li>\n\t<li>Supports EHS program to assure compliance with safety policies.</li>\n\t<li>Interprets results obtained during method development and troubleshoot tests as needed.</li>\n\t<li>Ensures compliance with current pharmacopeia, FDA and ICH guidelines.</li>\n\t<li>Updates specifications and test methods as needed.</li>\n\t<li>Provides scientific coaching to laboratory personnel, such as training in specific analysis techniques, protocol instructions, and method development technics among others.</li>\n\t<li>Prepares laboratory deviation reports.</li>\n\t<li>Performs any other duties as assigned.</li>\n</ol>\nEducation Requirement:\n\n<ul>\n\t<li>Bachelor's Degree in Chemistry (Analytical, Organic or Pharmaceutical).</li>\n\t<li>Eight (8) years of related experience in analytical laboratory.</li>\n</ul>\n\n<div>Experience Requirement:</div>\n\n<ul>\n\t<li>Experience in method validation (preparation of protocols and reports), analytical technology transfer and cleaning validation are required for pharmaceutical small molecules.</li>\n\t<li>Experience in a cGMP regulated analytical laboratory.</li>\n\t<li>Knowledge in FDA, ICH and USP requirements.</li>\n\t<li>Hands on experience in analytical method validations.</li>\n\t<li>Proficient in the use of LIMS system.</li>\n\t<li>Exercise attention to detail.</li>\n\t<li>Strong technical writing skills.</li>\n\t<li>Capable to read and interpret correctly scientific and technical literature.</li>\n\t<li>Excellent communication skills in English and Spanish.</li>\n</ul>\nWork Methodology:\n\n<ul>\n\t<li>100% On-site</li>\n\t<li>6 months (1st Contract)</li>\n\t<li>Administrative Shift (available to work flexible shifts, including weekends and overtime, as required).</li>\n\t<li>Temporary Contract</li>\n</ul>","hiringOrganization":{"@type":"Organization","name":"CIS International","sameAs":"https://condeinduservices.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Caguas, Puerto Rico","addressCountry":"Puerto Rico","addressRegion":"North America"}}}},{"@type":"ListItem","position":23,"item":{"@type":"JobPosting","title":"Laboratory Scientist","datePosted":"2025-07-21","description":"

Garvan Institute of Medical Research brings together world leading scientists and clinicians, collaborating locally and globally, to advance our understanding of disease, particularly cancer, autoimmunity and genetic disorders. Garvan is a global leader in fundamental biomedical research and its translation. Our mission is to make discoveries that will improve health for all.

THE OPPORTUNITY

The role involves working within the Cellular and Spatial Genomics Hub of the Garvan Genomics Platform overseeing and supporting the Platform’s workflow on cellular genomics assays. Services will be provided to internal, precinct, external and commercial researchers. Each assay has detailed SOPs which require following very carefully, and unexpected issues during experiments will need to be solved in a timely manner. While training will be provided, subsequent new developments/improvements will need to be learnt, and SOPs updated and developed.

The Laboratory Scientist role will be focused primarily on single cell genomic assays including: cell captures, library preparation, quantification and QC; project sample tracking with data recording; troubleshooting and protocol development and optimisation. You will have an opportunity to work with the Platform’s other Hubs – Flow Cytometry, R&D and Sequencing – to develop and test new exciting technologies in the genomics space, and there is also plenty of learning opportunity in the laboratory automation space. Attendance to local and international conferences is also offered where appropriate.

Garvan supports flexible working hours between 8 am and 6 pm, though there will be occasions where later start and finish times are necessary, dependent on the projects received.

Salary: Up to $86,000 + 12% superannuation + salary packaging (depending on experience)

Employment: 2-year fixed-term contract

SNAPSHOT OF BENEFITS

Generous salary packaging to save you income tax on your wages thereby boosting your monthly take home pay (max. $15,900 general expenses + $2,650 meals/accom)

Ample opportunities for on-going training and development

Stimulating, diverse and highly international research environment

Flexible work arrangements e.g. start / finish times

18 weeks paid parental leave for both parents including paid superannuation

A range of additional leave types to meet your personal needs including cultural leave, conference leave, community service and study leave

Discounted Health Insurance

Lifestyle discounts with our community partners

WHAT YOU WILL DO

ESSENTIAL DUTIES AND RESPONSIBILITIES

Responsibilities in this role include but are not limited to:

Perform Single Cell Genomics Assays:

Single cell/nuclei RNA sequencing (3’, 5’, VDJ, CRISPR, CITEseq, Flex)

scATAC-seq and sc Multiomics

Single Cell/Nuclei capture as per SOPs

Library construction and sample quality check (cells, nuclei, library)

Optimisation and implementation of new single cell platforms and technology

Execute all aspects of single cell/nuclei RNA sequencing platforms, including troubleshooting and communicate updates to customers in a professional manner

Establish and maintain excellent records of the molecular requirements and techniques for all projects handled by GGP.

Use of Airtable database and project tracking documents (e.g. Google sheets)

Assist in identifying areas of weakness in the GGP molecular analysis techniques and ensure the centre is adopting world best practices.

Regularly report to the team, Laboratory Manager, and GGP Lead on project progress and/or developments.

Training of new staff on:

All relevant aspects of GGP services

Different SOPs and technology

Safety and best practices

ABOUT YOU

The key skills and experience include:

BSc (Hons) or MSc in a relevant area of science, and understanding of genomics and molecular biology techniques.

Minimum 1 year of experience in a molecular biology lab.

Experience with single-cell technology is highly desirable.

Highly organised and excellent communicator.

The ability to assess priorities and manage competing deadlines.

Excellent written and oral communication, representation, and interpersonal skills to interact with internal and external stakeholders.

Excellent customer service capability.

Ability to manage competing responsibilities.

Ability to work independently and efficiently within a diverse team.

Strong creative thinking and problem-solving skills.

Display initiative/drive to take on primary tasks and provide additional support where
necessary.

ABOUT GARVAN

Garvan Institute of Medical Research is an independent Medical Research Institute (MRI) in Sydney, delivering scientific and clinical impact on a global basis and in partnership with organisations that share our vision. We are proud to be one of Australia’s largest and most highly regarded MRI’s.

Our vision is global leadership in discoveries to impact and our enduring purpose is to impact human health, by harnessing information encoded in our genome.

We seek to see our world-class discovery research achieve life-changing impacts, not only for individual patients with rare diseases, but for the many thousands affected by complex, common disease.

Garvan promotes a diverse workplace and is committed to the principles of equity, diversity, inclusion and belonging. We are always looking for culture ‘add’, not culture ‘fit’ and are building diverse teams with great sets of complementary styles and skills to help deliver our important work effectively.

HOW TO APPLY

To apply for this position, please submit your application with a CV and cover letter as one document, stating why you are interested in this role. We are reviewing applications as they are received. If you think you’re the right person for this role, we’d love to hear how your capabilities, achievements and experience set you apart. Only applicants with full working rights in Australia are eligible to apply for this role.

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Pay rate: $21.00 an hour

Bonus eligible: No

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs

Application window anticipated to close: 08/11/2025 *if interested in opportunity, please submit application as soon as possible.

What Nuclear Manufacturing contributes to Cardinal Health

Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment.

Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring.

Schedule:

40 Hours per week
Shift: This position operates both day and night shifts and requires working Sunday-Friday with start times varying from 9:00pm to a 10:00am with occasional weekend work
Candidate must be flexible to work different shifts, schedules, days and overtime as needed

Responsibilities

Successfully complete extensive training, including e-learning assignments and hands on components, to demonstrate and maintain proficiency
Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution)
Conducts quality control testing of each batch (utilizing gas chromatograph, dose calibrator, multi-channel analyzer, TLC plate scanner, high pressure liquid chromatograph, analytical balance, PTS, laminar flow hood and fume hood)
Works in ISO 7 cleanroom to make product vials and customer vials for use in drug production
Performs environmental and personnel monitoring in ISO 5, ISO 7, and ISO 8 environments
Coordinates daily production run schedule based on customer and pharmacy needs
Demonstrates strong documentation practices, oral communication, and writing skills. Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records
Manages SAP Inventory (includes receiving materials, properly inspecting materials for use, and maintaining proper cycle counts)
Performs daily radiation safety tasks, along with general lab cleaning

Qualifications

High school diploma, GED or equivalent or equivalent work experience, preferred. Education in Sciences (Chemistry, Biology etc. preferred).
0-1 years of experience preferred
Lab experience highly preferred
Must be able to work overnight shift (Facility operates at night.)
Prior experience in manufacturing, preferably in a controlled environment and/or regulated industry desired.
Effective written and verbal English communication skills
Able to repeatedly follow detailed processing instructions
Ability to manage several tasks at the same time; Ability to evaluate operating conditions and exercise sound judgment and problem-solving skills.
Ability to manage up to 75 pounds as needed
Ability to see fine particulate and differentiate colors in liquid solutions.
Ability to hear, write (English), and speak (English) clearly in order to communicate in manufacturing setting.
Manual dexterity required for equipment operation and occasional reach and lifting of small objects.
Ability to be an effective team member.
Comfortable working in a nuclear environment
Ability to work weekends or be in a weekend rotation
Ability to work holidays or be in a holiday rotation
Ability to travel up to 10 percent
Ability to work overtime with little or no advance notice

What is expected of you and others at this level

Applies basic skills and techniques to complete routine tasks within assigned area
Maintains appropriate licenses, training and certifications
Works on basic and routine assignments
Works within clearly defined Standard Operating Procedures and/or scientific methods
Adheres to all quality guidelines
Works under close supervision
All work is reviewed for accuracy
Any deviations from the norm are approved by the supervisor before proceeding
10 percent travel

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

To read and review this privacy notice click here

","hiringOrganization":{"@type":"Organization","name":"Cardinal Health","sameAs":"https://cardinalhealth.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"NV-Las Vegas PET 2, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":25,"item":{"@type":"JobPosting","title":"Laboratory Manager","datePosted":"2025-07-21","description":"

Job Family:

Laboratory Technician (Digital)

Travel Required:

None

Clearance Required:

Ability to Obtain Public Trust

What You Will Do:
We are currently searching for a Laboratory Manager. This role will provide support services to satisfy the overall operational objectives of the National Heart, Lung, and Blood Institute. The primary objective is to provide services and deliverables through the Hematology Branch (HB). This is a full-time opportunity located in Bethesda, MD.

Coordinate and support the design, execution, and analysis of laboratory experiments in alignment with the lab’s scientific objectives.
Collaborate with researchers on assay development, method optimization, and interpretation of experimental results.
Lead the training and mentoring of laboratory staff, postdoctoral fellows, and interns in molecular biology, biochemistry, and analytical techniques such as qPCR, Sanger sequencing, flow cytometry, and DNA/RNA extraction.
Ensure adherence to protocols and promote a culture of safety and scientific rigor.
Oversee daily lab operations including procurement of supplies, equipment maintenance, vendor coordination, and compliance with safety and regulatory standards.
Maintain laboratory documentation, safety manuals, and chemical hygiene plans.
Manage the lab’s operating budget, track expenditures, and coordinate funding requests.
Handle purchasing external services such as genetic testing and ensure financial accountability for clinical and research activities.
Supervise the processing, storage, and inventory of clinical and research samples using systems like BSI and CRIS.
Ensure accurate recordkeeping for specimen tracking, cell counts, and freezing media. Coordinate sample shipments to national and international collaborators.
Maintain and troubleshoot scientific instruments including HPLCs, spectrophotometers, centrifuges, and genetic analyzers.
Train staff in proper use and ensure calibration and functionality of all lab equipment.
Serve as the lab’s liaison for inspections and audits.
Prepare and submit animal study protocols and ensure compliance with institutional and federal guidelines.
Update research project registrations and documentation for annual reviews.
Analyze and interpret research data; contributes to the preparation of abstracts, presentations, and manuscripts.
Conduct statistical and bioinformatics analyses to support publication and grant submissions.
Participate in lab meetings and planning sessions to guide future research directions.
Collaborate with internal departments, external partners, and research monitors to ensure alignment of resources and compliance with study protocols.
Represent the lab at scientific conferences and external meetings, particularly in areas related to bone marrow failure diseases.
Lead onboarding and instruction for visiting students and fellows, fostering a collaborative and inclusive research environment.

What You Will Need:

Master’s degree in Biology, Chemistry or a related discipline OR Bachelor’s Degree plus FOUR (4) years of specialized experience is equivalent to a Master’s degree.
A minimum of EIGHT (8) years of laboratory experience.
General experience with basic biochemical and molecular biologic techniques, with an understanding of the general scientific principles.
Proficiency in site-directed mutagenesis and basic protein biochemistry.
Strong communications skills, both oral and written.
Excellent analytical, organizational and time management skills.

What Would Be Nice To Have:

Previous experience with NIH preferred.
Ability to be self-motivated, detail oriented and have strong organizational skills.

The annual salary range for this position is $113,000.00-$188,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.

What We Offer:

Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.

Benefits include:

Medical, Rx, Dental & Vision Insurance
Personal and Family Sick Time & Company Paid Holidays
Parental Leave
401(k) Retirement Plan
Group Term Life and Travel Assistance
Voluntary Life and AD&D Insurance
Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts
Transit and Parking Commuter Benefits
Short-Term & Long-Term Disability
Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities
Employee Referral Program
Corporate Sponsored Events & Community Outreach
Care.com annual membership
Employee Assistance Program
Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)
Position may be eligible for a discretionary variable incentive bonus

About Guidehouse

Guidehouse is an Equal Opportunity Employer–Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.

Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.

If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.

All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or guidehouse@myworkday.com. Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.

If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse’s Ethics Hotline. If you want to check the validity of correspondence you have received, please contact recruiting@guidehouse.com. Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant’s dealings with unauthorized third parties.

Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.

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Job Description

happen. We appreciate our peoples’ courage, curiosity and unique perspectives, and look to collaborate as much as possible to explore safer, smarter and more efficient ways of working in this rapidly changing world. We don’t stand still – there are always opportunities to do more and do better.

Keen to progress your career? Take full advantage of our tailored training, leadership, and mentoring programs; or leverage our partnerships with industry association such as Engineers Australia, Chartered Accountants, CPA Australia, Infrastructure Sustainability Council, The National Association of Women in Construction, plus many more.

Looking to enhance your wellbeing? We will encourage you to explore flexible working arrangements where possible. We offer great benefits, including corporate health and fitness programs, health insurance discounts, personal banking support, a range of retailer discounts, up to 18 weeks paid primary carers parental leave and up to 10 days paid secondary carers leave, access to our Employee Assistance Program (including your immediate family), and the option to take more time for yourself throughout the year with our Purchase Leave Policy.

Want to help us better the communities we live and work in? Our purpose of creating, connecting, and caring for communities is more than a saying to us – it’s a way of thinking, working, and living because we're locals too, and seek to give back in ways that strengthen and build resilient communities. We do this because we genuinely care, enjoy what we do, and even manage to have some fun along the way! You’ll find us partnering with local and national community groups, like Clontarf Foundation, Black Dog Institute, and Soldier On, in addition to indigenous groups and social enterprises, to ensure that our good work positively impacts and brings about sustainable change within our industry.

Do we offer a ‘competitive’ salary package? Of course! Speak to our Talent Acquisition or People & Culture team to learn more.

What’s on offer?

An exciting opportunity for an experienced Quarry Laboratory Supervisor has become available to join our Northern Region Infrastructure Services Team based in Cedar Creek.

In this role you will be responsible for:

Quarry laboratory operations based at Cedar Creek, including team supervision and development, and laboratory assets.
Ensure OH&S compliance, risk (SMWS, et., al), quality and calibration compliance for the laboratory.
Ensuring laboratory and production facility compliance with NATA, and Department of Main Roads Construction Materials Testing Supplier Registration System, together with all statutory health, safety and environmental requirements.
Assist in the design and performance of laboratory mix designs/ blends & quarry R&D to the required specifications.
Supervise, train and undertake compliance testing for samples of aggregate, soils, road base, and CTB materials.
Record, report and data/process control for product performance tracking.

As the successful candidate, you will hold a high level of competence and experience in Quarries Construction Laboratories including, NATA signatory status for test methods.

This is a fulltime position, with occasional weekend work.

In addition, you will be able to demonstrate:

Extensive quarry experience, soils and road materials knowledge and experience, including skills in research, evaluation, interpretation and delivery of data.
Sound knowledge of Queensland test methods and Aggregates and Soil Australian standards for laboratories with a keen eye for detail.
Proficiency in the Microsoft Office Suite and Questlab.
Proven record and ability to thrive in a quarry fast-paced environment.
Strong leadership skills with a commitment to collaborative, ethical behaviour in a client-facing environment and an ability to communicate across all levels of the business.
Ability to interpret and apply policies, procedures, and relevant legislation.

Our people share the same set of values that keep us REAL. Respect, Energy and Effort, Attitude and Leadership encapsulate what we stand for at Fulton Hogan and encourage us to foster a diverse and inclusive culture where we listen to, care for, celebrate, and respect everyone. If our values resonate with you, please submit an application for the position. If you’re not sure that you meet 100% of the selection criteria, that’s okay, we would still like to hear from you and potentially discuss how your skills could be utilised at Fulton Hogan.

For 90 years, Fulton Hogan has been delivering high-quality infrastructure to improve the lives of people every day. Our 10,000+ team works in every kind of weather and environment, creating, connecting, and caring for communities across Australia and New Zealand.

We celebrate and embrace diversity across our business and are committed to equal employment opportunities.

We believe in the value that diversity brings to our team and people who share our REAL values are encouraged to apply.

","hiringOrganization":{"@type":"Organization","name":"Fulton Hogan","sameAs":"https://www.fultonhogan.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"QLD Blue Rock, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":27,"item":{"@type":"JobPosting","title":"Laboratory Supervisor","datePosted":"2025-07-21","description":"

Job Description

Role Title: Laboratory Supervisor

Location: Alexandra, Central Otago

Contract Type: Permanent - Full Time

The Fulton Hogan Life

Life at Fulton Hogan is about making the most of the opportunities, taking responsibility, having a crack, being accountable and making it happen. We live by our REAL values – Respect, Energy & Effort, Attitude, Leadership – and we demonstrate these through the good work we do, every day, as one team.

Nau mai haere mai ki tā mātou whānau |Welcome to our Fulton Hogan Family

We have a rare and exciting opportunity for a Laboratory Supervisor to join our Central Testing Services team based in Alexandra. As a Laboratory Supervisor, you will be responsible for the workflow of the aggregates, soils, concrete and asphalt testing areas, ensuring the laboratory staff assigned to your area are efficiently utilized, trained and developed. Ensuring all client needs are met and results are delivered in a timely manner is a large part of this role. You will also apportion time, to further support the laboratory team by actively carrying out laboratory testing.

In addition to the above you will:

Be responsible for ensuring that all equipment and operations are utilised or conducted in a safe and environmentally compliant manner.
Undertake the day-to-day operations of the laboratory, working cooperatively with the Field and Administration Supervisors, as needed to ensure all work is completed to the required standards.
Ensure all lab-based testing is completed in a safe manner and in line with Fulton Hogan policies and procedures.
Gain an understanding of the laboratory financial reporting requirements to ensure all work and reporting is completed and delivered in a timely manner.

Good Work equals Good Benefits

Medical insurance
Life insurance
KiwiSaver employer contributions after service milestones up to 7%.
Fuel discount card.
Family scholarships.
Ongoing training and development, career growth and progression opportunities.
Great discounts at a wide range of retailers.

At Fulton Hogan, we genuinely care about the wellbeing of our people and giving them the tools and opportunities they need to succeed and grow with us.

We’re looking for someone with:

Minimum 3 years’ experience working in a civil engineering laboratory.
Tertiary or trade qualification or similar.
Excellent communication skills – build strong relationships based on honesty, delivering on promises in a positive and friendly style with the laboratory team, internal and external clients, suppliers, service providers, subcontractors and compliance organisations such as IANZ, MOH, Worksafe and ORC.
Proficient in the use of MS Office suite particularly Word, Excel, Outlook.
Excellent time management skills with ability to prioritize own workload.

Creating, Connecting and caring for the community

Our people regularly donate their time to local causes and initiatives, while at a regional and national level we provide financial support, skills and resources to a wide range of organisations that are strengthening our communities. Our focus aims to also reduce our impact on the environment, and regenerate healthy new ecosystems. We look to partner with others to lift the standards of our industry and show customers lower-impact, sustainable ways of delivering infrastructure.

Learn more about us: Homepage - Fulton Hogan and make an application to join our growing industry.

All successful candidates must under-go and pass a pre-employment medical and drug screen prior to employment.

All successful candidates must under-go and pass a pre-employment medical and drug screen.

We celebrate and embrace diversity across our business and are committed to equal employment opportunities.

We believe in the value that diversity brings to our team and people who share our REAL values are encouraged to apply.

","hiringOrganization":{"@type":"Organization","name":"Fulton Hogan","sameAs":"https://www.fultonhogan.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"OTA Central Testing Alexandra, New Zealand","addressCountry":"New Zealand","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":28,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-07-21","description":"

Conduct IR/TGA/DSC/IC tests on samples according to standard requirements, work instructions and equipment usage manual, record observed and calculated data on testing datasheet.
Review test spectrum to judge if it match the information provide by client, and effectively communicate with project handler and client.
Establish Spectrum database, and retain test samples.
Performs routine maintenance of designated test equipment and laboratory area.
Support Lab manager/supervisor on new testing capability build up, be familiar with testing standard, work instructions, etc.
Provides feedback and may assist in development of laboratory procedure guides (LPG)
Demonstrated ability to manage multiple projects while maintaining high quality and exceptional customer service
Integrates continuous improvement concepts and techniques into all aspects of the job.
Resolves engineering issues associated with Variation Notices by analyzing and reporting on the acceptability of the variations
Performs other duties as directed.

根据标准要求、作业指导书和设备使用手册对样品进行IR/TGA/DSC/IC测试，将观察到的和计算的数据记录在测试数据表上。
对测试谱图进行分析，判断是否与客户提供的信息相符，并与项目负责人和客户进行有效沟通。
建立谱库，保存测试样品
对指定的测试设备和实验室区域进行日常维护。
支持实验室经理/主管建立新的测试能力，熟悉测试标准，作业指导书等。
有能力管理多个项目，同时保持高质量和卓越的客户服务。
将持续改进的概念和技术融入到工作的各个方面。
通过分析和报告变更的可接受性，解决与变更通知相关的工程问题
执行主管其他指定的职责。

Science and engineering, bachelor degree, major in chemical/material science is preferred.
At least 1 years working experience.
Good management skills of multiple projects.
Good English skills in reading and writing.
Good communication and collaboration skills.
Working experience about material testing is preferred

化学相关专业，本科，高分子材料，分析化学相关更佳。
至少一年工作经验，优秀的应届生亦可。
良好的英语读写能力。
良好的沟通和协作能力。
有材料分析相关经验者更佳。

A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.

","hiringOrganization":{"@type":"Organization","name":"UL Solutions","sameAs":"https://www.ul.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"China","addressCountry":"China","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":29,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-07-21","description":"

Essential Functions:

Perform Mechanical laboratory testing for Fastener samples to pre-determined test methods
Adhere to procedures to ensure compliance to NADCAP, AS9100 and customer requirements
Understand and interpret technical documents with demonstrable experience of at least 1 year in a similar role.

Specific Responsibilities Include:

Key responsibilities include

Destructive testing of samples for production batches. Test methods include;
- Tensile
- Double Shear
- Proof stress and elongation
- Fatigue
- Chemical analysis
- Torque
- Metallurgical assessments

Accurately recording test data and transposing to the ERP system.
Exporting reports from test machines to the ERP system.
Participation in Internal Round Robin program.
Identifying and reporting errors in testing

Other Duties and Responsibilities

Participation in NADCAP audits.
Liaison with Logistics team to process priority WIP in a timely manner.
Development of internal procedures for test methods.

Equipment Used:

ERP system

Microsoft Excel

Microsoft Outlook

Test machine control software

Must have at least 1 year of experience in a manufacturing/lab environment
Experience is essential in a quality-based role (i.e. inspection or test technician
Must have great attention to detail.
Must be able to read technical drawings and specifications.
Demonstrable skills in escalating problems that are identified in the testing procedure
Experience of working as part of a team

Physical Demands

The role involves the destructive testing of product. As such you will be required to perform physically repetitive tasks such as loading jigs to test machines, loading samples to jigs and preparing micro cross section mounts.

Technical Demands

You will be required to follow specific test instructions and be capable of interpreting product technical specifications for test parameters.

\n\n Howmet Aerospace Inc. (NYSE: HWM), headquartered in Pittsburgh, Pennsylvania, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries. Our primary businesses focus on jet engine components, aerospace fastening systems, titanium structural parts and forged wheels. With $7.4 Billion in revenue in 2024, our products play a crucial role in enabling fuel efficiency and lightweighting, contributing to our customers’ success and making a positive impact on the world. To learn more about the way Howmet Aerospace Inc. is advancing the sustainability of our customers, markets, and communities where we operate, review the 2024 Environmental Social and Governance report at www.howmet.com/esg-report. Follow: LinkedIn, Twitter, Instagram, Facebook, and YouTube.","hiringOrganization":{"@type":"Organization","name":"Howmet Aerospace","sameAs":"https://www.howmet.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Redditch, HEW, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":30,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-07-21","description":"

Laboratory Technician

Location: ZRECE, Slovenia

Application closing date: 30.08.2025

GKN Driveline Slovenia - your next career step?

At GKN Driveline Slovenia, excellence isn’t just a goal – it’s our standard. We deliver top-tier quality through precision, innovation, and a deep-rooted passion for automotive engineering. Our people are our greatest asset, which is why we invest in their well-being, safety, and growth every step of the way. We’ve built a workplace where health, trust, and opportunity thrive – because when our employees succeed, so does our business. Join a company where your talent drives real impact, and your future is built on purpose.
If you wish to work for a stable company that you can commit to long-term, but also take part in dynamic projects and scale-up your learning and career development then GKN Automotive might just be your next career step!

Role overview

You will be performing physical and metallurgical measurements, verification of materials, components and assemblies during each stage of development and manufacture. You will also support product audits, development, maintenance, and improvement of measurement systems to ensure valid results.

Key Responsibilities

Improvement / Innovation: Support the development, maintenance, and improvement of measurement systems and procedures to ensure valid results.
Operational Compliance: Support the definition of procedures for each laboratory activity (measurement, instrument programming, test, calibration) and ensure compliance to external measurement standards and related GKN specific requirements.
Quality Inspection: Perform required inspection, instrument programming, test, or calibration according to the defined procedures.
Data Collection and Analysis: Support internal and external reports for product/process validation, material approval, and customer specific issues or requests. Retain appropriate documented information and test samples as evidence of the results.
Audit Compliance: Provide measurement services and perform Product Audits to ensure compliance to product specification at all stages of manufacture.
Process Reporting: Support internal and external reports for product/process validation, material approval, and customer specific issues or requests. Retain appropriate documented information and test samples as evidence of the results.

Qualifications & Skills needed to succeed in this role:

Experience: Experience in a similar role
Education: Metallurgy
Language Skills: Intermediate English
Other Skills: Verbal Communication, Data Collection and Analysis

Why Join Us?

Joining our team as a Laboratory Technician means stepping into a world of innovation, precision and purpose. If you are passionate about technology, eager to learn and ready to make a real impact, we are the right place for you!

We provide a competitive compensation and benefits package, including:

Competitive annual holiday bonus
Benefits: Competitive pay
Career Growth: Opportunities for long-term career development and professional growth in a stable company.
Advanced Certificate as a Socially Responsible Employer
Industry Leadership: Join a market-leading company with strong potential for ongoing growth.
Employee events, team – building activities
Structured onboarding and mentorship program

NOTE: Please submit your resume in English because we are an international environment, and English is our business language.

\nGKN Automotive is the market leader in conventional, all-wheel and electrified drive systems and solutions. With a comprehensive global footprint, we design, develop, manufacture and integrate an extensive range of driveline technologies for over 90% of the world’s car manufacturers. As a global engineering company, innovation is what differentiates us from our competitors and is central to our success. A balance of cultures, ethnicities and genders help bring new ideas and creativity to GKN Automotive. We need people of different backgrounds, with different skills and perspectives to spark originality, imagination and creativeness in our teams around the world. GKN Automotive is an equal opportunity employer. We treat all our employees and applicants fairly and are committed to ensuring that there is no discrimination or harassment against any employee or qualified applicant on the grounds of age, race, creed, colour, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please contact us to request any such accommodation.","hiringOrganization":{"@type":"Organization","name":"GKN Automotive","sameAs":"https://www.gknautomotive.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Zrece, Slovenia","addressCountry":"Slovenia","addressRegion":"Europe"}}}},{"@type":"ListItem","position":31,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-08-01","description":"

Company Description

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Responsible for helping maintain cleanliness and supply levels in lab

Essential Duties and Responsibilities:

•   Demonstrates and promotes the company vision
\n•   Regular attendance and punctuality
\n•   Clean, dry, and store glassware for laboratory use
\n•   Dispose of waste solutions
\n•   Retrieve washroom acids and solvents
\n•   Clean and maintain glassware areas
\n•   Learn simple laboratory operations such as media production
\n•   Learn and use inventory and ordering system for lab supplies
\n•   Assist with receiving and placing lab supplies in proper place
\n•   Perform sample preparation
\n•   Assist with sample registration as needed
\n•   Conducts all activities in a safe and efficient manner
\n•   Performs other duties as assigned
\n

Qualifications

HS diploma or equivalent
Willingness and ability to work overtime, weekends and occasional holidays
Authorization to work in the United States indefinitely without restriction or sponsorship
Able to work both independently and in a team.
Regular attendance and punctuality
Able to handle fast paced, high through-put environment and potential stress
Able to handle food testing and everything that entails (smells, rotting food, etc)
Able to stand for approx 8 hour shift
Able to perform repetitive tasks consistently and accurately

Additional Information

Shift: 2nd Shift (3pm-11:30pm) Mon.-Fri., Tues.-Sat. or Sun.-Thurs. Candidates currently living in a commutable distance to Lancaster, PA. are encouraged to apply.

Pay Range: $14/Hr.- $17/Hr.

Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Lancaster, PA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":32,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-08-02","description":"

Laboratory Assistant at Providence St. Joseph Medical Center in Burbank, CA. This position is per-diem and will work variable shifts.

Collects blood from patients, coordinates and processes specimen collection following established standards and practices.

Required Qualifications:

Education to meet certification, license or registration requirement.
Phlebotomy experience.
2 years Experience in the health care field in related work.

Why Join Providence?

","hiringOrganization":{"@type":"Organization","name":"Providence","sameAs":"https://www.providence.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Burbank, CA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":33,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-07-16","description":"

ABOUT YOU

As the Lab Technician, you will be an individual with an aptitude for learning who is looking to kickstart their laboratory career with a high commitment to quality service delivery through continuous improvement.

Required skills and experience:

Academic background in science or previous experience in a laboratory role is beneficial, but not essential.
Good IT literacy skills, especially in Word and Excel.
Good time management skills, with a flexible approach to working.
Ability to follow both oral and written instructions.
Ability to work with others in a cooperative manner.
Conscientious with good documentation skills.
Driving license desired but not essential.

ABOUT THE OPPORTUNITY

The role includes but is not limited to; In-Vitro testing, supporting in the laboratory on outsourcing projects, comprehension use of database systems and administrative procedures.

Key activities:

Perform routine and non-routine analytical tasks as part of the in vitro assessment of oral care products.
Use a variety of cutting and abrading equipment to prepare hard tissue samples.
Maintain documentation to meet the requirements of our quality management system.
Perform data entry and data checks in accordance with standard procedures.
Maintain and calibrate equipment in accordance with standard procedures.

WHAT WE OFFER

Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.

Competitive salary/benefits
Development and career opportunities around the Globe
Working in a highly motivated team and dynamic working environment

We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.

Intertek operates a preferred supplier arrangement and we do not accept unsolicited approaches from agencies.

","hiringOrganization":{"@type":"Organization","name":"Intertek","sameAs":"https://www.intertek.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Cheshire, England, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":34,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-01","description":"

Company Description

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Completes routine laboratory procedures such as but not limited to preparation of solvents, buffers, media, mixing of chemicals, etc.
Reports timely and accurate test results according to laboratory policies and procedures
Follows GDP standards for all documentation.
Routine maintenance of lab instruments and troubleshooting.
Stores chemicals properly, disposes of chemical waste, adheres to safety procedures, and participates in safety programs.
Manages inventory, maintains laboratory supplies including glassware and chemicals for biotech/pharmaceutical processes.
Tracks and documents chemical usage and inventory.
Maintains clean room to prevent contamination and integrity of production.
Operates laboratory equipment and instruments.
Calibrate balances and pH meters.
Inspect laboratory safety stations.

Qualifications

Bachelors degree in a scientific concentration
1-2 years’ experience in a laboratory setting and understanding of laboratory equipment a plus
GxP training a plus
Valid Driver’s License and transportation
Conform to all customer requirements for background checks, health and safety issues, security clearances and medical checkups
Requires knowledge in using various instruments to prepare for and perform tests
Authorization to work in the United States indefinitely without rescritctions or sponsorship

Additional Information

Position is full-time, Monday - Friday 7am-3:30pm. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Malvern, PA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":35,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-08-01","description":"

HealthPartners is hiring for a Lab Assistant working in the Central Lab.

QUALIFICATIONS:

REQUIRED:

High School Diploma or equivalent.

One year computer navigation and computer experience with Microsoft Office products (Word and Outlook) or comparable applications.

Typing or keyboarding skills.

Promote teamwork through demonstration of a courteous and cooperative attitude to all customers.

PREFERRED:

Six months of related medical training, medical terminology or related experience.

Previous phlebotomy experience.

PHYSICAL REQUIREMENTS:

Ability to sit or stand for prolonged periods of time. Must possess speech, hearing and sight skills to perform the functions of the position. Manual dexterity required. Must be able to speak, read and write English proficiently. Some lifting may be required.

POSITION PURPOSE:

Service excellence is to be centered on patient care and patient relationships and is the responsibility of all employees. Teamwork is the norm and all employees will be held accountable to work as effective team members. This individual serves all (internal and external) customers by performing laboratory procedures and support functions in accordance with HealthPartners philosophy, policies and procedures and in accordance with all regulatory agencies.

ACCOUNTABILITIES:

1. Collect and process biological specimens with appropriate techniques following established Standard Operating Procedures (SOP).

2. Perform testing analysis and verify assay/analyzer performance according to SOP in an efficient cost effective manner. Any combination of the following areas may be included: Phlebotomy, computer operation, EKG, reception, telephones, clerical and designated testing procedures

3. Document and communicate lab test results thoroughly and accurately according to SOP.

4. Perform and document maintenance procedures plus maintain adequate supplies.

5. Demonstrate competency and comply with all regulatory agency policies.

6. Consistently implement and adhere to the laboratory customer service standards. The standards include maintaining confidentiality, promoting teamwork, successful communication and conflict resolution.

7. Respond proactively to stressful circumstances, customer needs and department/clinic changes.

8. Demonstrate professional development through participation in continuing education, special projects and community / corporate / professional organizations. Demonstrate personal development through dependability, professional appearance and cooperative attitude.

9. Perform other duties as assigned.

\n\n

122480 Laboratory Assistant Page 2 of 2

\n\n

Join us in our mission to improve the health and well-being of our patients, members, and communities.

","hiringOrganization":{"@type":"Organization","name":"HealthPartners","sameAs":"https://www.healthpartners.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Eden Prairie, MN, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":36,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-02","description":"

Description

Job title: Lab Technician

Reports to: Lab Manager

Level: Individual Contributor

Classification: Non-exempt

Status: Regular Full Time

Job Purpose

Lab Technicians perform routine laboratory tests under close supervision to determine chemical or physical characteristics of samples. Lab Technicians ensure that their duties are completed accurately and delivered with high quality in a timely manner.

Duties and Responsibilities

• Perform basic analytical tests based on standards and procedures as assigned by the Laboratory Manager.
• Assist and perform the setting up, adjusting and operating laboratory equipment.
• Calibrate laboratory instruments as needed to ensure that analysis is accurate according to the Quality Management systems.
• Clean and sterilize laboratory equipment.
• Prepare chemical solutions according to standard formulas.
• Records test results on standardized forms and writes test reports describing procedures used.
• Understand and complete laboratory raw data sheets and make accurate entries into LIMS data base.
• Ability to read and comprehend all analysis as well as safety standards in English, including ASTM, UOP, IP and other well-defined analytical standards and procedures used in the laboratory.
• Exercise procedural, safety and quality requirements specified in Laboratory Manual & Safety Manual and company policies.
• All other duties assigned by management.

Other Duties

• Management reserves the right to change job duties with or without notice.

Qualifications

• Bachelor’s Degree in Chemistry or a related science preferred, or equivalent work experience; coupled with a minimum of one (2) year of direct transferable experience working in a laboratory.
• Knowledgeable in ASTM standards.
• Must be able to work with all chemical, petrochemical and petroleum products.
• Must be able to differentiate between colors accurately by sight.
• Laboratory Information Management System (LIMS) experience preferred.
• Proficient in MS Word, Excel, Access preferred.
• Have a great work history with a track record of being responsible individual.
• Detailed orientated.
• Excellent communication skills.
• Proficient in the use of laboratory equipment.

Travel

Travel is not required for this position.

Working conditions

This position is performed in a Laboratory environment.

Requirements

Physical requirements

The working environment and physical demands described here are representative, but not necessarily all-inclusive, of those that must be met by an employee to successfully perform the essential functions of this job.

• Required to walk, sit, and reach with hands and arms; and to stoop, kneel, crouch, crawl, or twist body to fit and/or reach.
• The employee’s lifting requirement and/or move items up to 50 pounds.
• Be able to work in the presence of odors typical of petroleum or petrochemicals without allergic reactions or nausea, when such odors are within OSHA-designated permissible exposure limits (PELs).
• May be exposed to fumes, airborne particles, and toxic or caustic chemicals.
• The noise level in the work environment is usually moderate.

AAP/EEO: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, or national origin.

","hiringOrganization":{"@type":"Organization","name":"Coastal Gulf & International","sameAs":"https://www.coastalgulf.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Saint James, LA, US","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":37,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-07-03","description":"

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In 2024, Eurofins generated total revenues of EUR € 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins BioPharma Product Testing Australia / New Zealand provides contract GMP testing to human and animal pharmaceutical, biotechnology, medical device and complementary medicine manufactures, as well as an extensive range of SPF and other cosmetics testing, both in-vitro and in-vivo in accordance with a range of local and international standards. The range of testing includes microbiological and chemistry on raw materials, in process and finished products, complemented by product formulation services. We operate out of two main sites in Sydney and Auckland, with two satellite operations in Melbourne and Brisbane. All our sites are GMP licensed by local regulators and are accredited to ISO 17025. In addition to the provision of world class analytical testing, the laboratories also provide consultative services to their clients made available by a team of highly qualified scientists.

Job Description

Operating in the south eastern suburbs of Melbourne, this modern contract-testing laboratory is seeking a full time Laboratory Technician with a Wet Chemistry background for an immediate start.

Accredited with the TGA and APVMA, the high-tech facilities encompass a broad range of analytical equipment primarily used in the Pharmaceutical, Veterinary and Bioanalytical sectors.

The successful candidate will be self-motivated with a positive attitude, willingness to learn on the job in a fast-paced, friendly environment with a dedicated team of like-minded professionals. Advancement opportunities may exist for the right candidate.

Candidates will be expected to keep the laboratory well stocked with consumables and maintain the Kanban system and to prepare common reagents and buffers as well as perform TOC, Nitrates Conductivity and Karl Fisher testing on pharmaceutical samples. Candidates should also possess the ability to perform basic routine pharmacopeial testing (USP, BP/EP) on both raw materials and finished products. The position relies heavily on current or developed expertise in analytical chemistry, with sound analytical techniques and attention to detail. Experience in techniques such as pH, Karl Fisher, UV-Vis, FTIR, Polarimetry, Melting Point are also advantageous.

Qualifications

At a minimum, a diploma in Chemistry, Analytical Science or a related discipline is essential, as well as at least 1-3 years experience working within a TGA Licensed Laboratory. High performing graduates also encouraged to apply.

Ability to multitask.
Excellent verbal and written communication skills.
Ability to work within a team with minimal supervision to tight timelines.
Sound Report writing skills will round out the desired qualities sought for this position.

Imperative to the successful operations of this highly respected testing facility is a strict understanding and adherence to the cGMP quality system, consideration of time-sensitive workloads and the accurate and thorough recording of all results, activities and deviations encountered during the varying stages of analysis.

Additional Information

If you feel that you can bring outstanding skills and a great attitude to our team, please submit a cover letter, curriculum vitae and be able to provide at least two recent professional references. Applications will be treated with the strictest confidence.

This opportunity is only open to candidates who are eligible to work in Australia/New Zealand, and already have work rights or an appropriate working visa.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dandenong, VIC, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":38,"item":{"@type":"JobPosting","title":"Laboratory Leader","datePosted":"2025-06-30","description":"

Job Location

READING PLANT

Job Description

P&G is one of the world’s largest consumer goods companies owning global brands such as Gillette, Fairy and Oral-B. We hold true to our purpose, values and principles as we seek to make a difference in the world around us. We’re looking for a Laboratory Leader to join our team at our Gillette manufacturing facility in Reading.

As Laboratory Leader you will be responsible for leading the Laboratory Team, driving continuous improvement through loss elimination, problem solving and growing the capability of the Lab Team. You will be accountable for helping to ensure our products, processes and standards meet regulatory and Good Manufacturing Practice requirements as well as the commercial expectations of the business.

Important Responsibilities on a day-to-day level:

Career and performance management of the Laboratory Team (consisting of 6 Lab Analysts)
Overall ownership of the training program of the Lab Team and ensuring a positive onboarding experience for new hires
Ensuring all corporate and regulatory requirements are met in the Analytical Lab with regards to Safety, Quality and Stewardship
Fostering a winning culture in the Team by increasing release reliability and improving the health of the Laboratory Management System
Playing a crucial role in driving zero-loss mentality by owning the lab score card and lead gap analysis on any targets not being met
Leading and improving the daily direction setting in the Laboratory to ensure the team are clear on their roles and responsibilities

What we offer you:

Competitive Salary and Benefits: The starting salary for this role is competitive, every P&G employee’s salary is reviewed annually and therefore there is ample opportunity for future salary increases. P&G take a Total Rewards approach meaning on top of your salary, you can expect a whole range of benefits including a double-matched pension scheme, private health insurance, and your very own ‘Flex4Me’ Fund which enables you to allocate a portion of your benefits package to the areas that matter most to you.
Generous Pension: The Company will contribute double the amount you contribute towards your pension savings, up to a maximum company contribution of 14% of your pensionable pay.
Annual Leave: You will start with 25 days' annual leave entitlement (plus bank holidays), increasing with length of service up to 30 days.
1-4-1 Shares: For every share that you purchase, the Company will purchase a share on your behalf. You can contribute up to 2.5% of your salary into the 1-4-1 Share Plan, up to a maximum of £150 a month.
Great Working Environment: Gillette has had operations in Reading since the 1950s and the site is of great importance for the company. On-site we offer a friendly work environment with lots of great local benefits such as a free onsite gym, discounted restaurant, free parking, Occupational Health support, local events and more!

Job Qualifications

What we are looking for:

Leadership: The successful candidate demonstrates leadership and people management skills with the ability to lead cultural change. We are looking for positivity, \"can-do\" attitude as well as a passion for getting things done.
Technical Mastery: Analytical expertise and good understanding of Laboratory GMP practices are essential. Existing knowledge of gas chromatography is desirable. The successful candidate has experience working in a Lab environment or Quality Assurance (QA) organization.
Communication: Strong communication skills, both written and verbal are desirable. The successful candidate can communicate well internally and externally across different levels of the organization. This includes the ability to escalate issues when needed to remove barriers.
Collaborative Relationships: Strong collaboration skills are critical to support the Operations and other Departments on site. The successful candidate demonstrates the ability to network and leverage existing analytical knowledge, expertise and best practices across P&G.
Problem-Solving + Loss Elimination: The successful candidate has a strong “zero loss” mentality and takes full ownership of losses in the Lab to drive testing reliability. We are looking for a candidate with the ability to coach the Lab Team during investigations, trouble-shooting issues with Lab instruments and root causing out-of-spec results.
Systems: A working knowledge of Quality systems which are used regularly as part of the Lab work (such as SAP, ENOVIA, VEEVA, Chromeleon, NEXUS LIMS or Proficy Quality) is desirable though not essential as on the job training will be provided.

Right to Work
For this role, P&G are willing to provide sponsorship to those who require a visa to live and work in the UK, subject to meeting all the necessary Home Office requirements. Full details on visa restrictions can be found on the Home Office website and immigration rules are subject to change.

P&G is legally required to ensure all candidates have the right to work in the UK from Day 1 of their employment. All applicants will therefore be asked to provide evidence of their right to work at the conclusion of the recruitment process as a condition of employment.

At P&G #weseeequal
We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work.

Job Schedule

Full time

Job Number

R000134237

Job Segmentation

Experienced Professionals (Job Segmentation)","hiringOrganization":{"@type":"Organization","name":"Procter & Gamble","sameAs":"https://pg.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"READING PLANT, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":39,"item":{"@type":"JobPosting","title":"Laboratory Supervisor","datePosted":"2025-07-21","description":"

Description

GENERAL SUMMARY

The Laboratory Supervisor under the direction of the Medical Laboratory Director the Laboratory Manager is responsible for managing laboratory technical staff, monitoring processing of medical specimens, maintaining laboratory supplies inventory and knowledge of and compliance with accrediting agencies policies and regulations.

ESSENTIAL JOB FUNCTION/COMPETENCIES

Responsibilities include but are not limited to:

Manage all laboratory staff daily. Monitor work practices and ensure all stated policies and procedures are followed.
Monitor receipt, processing and eventual reporting of all specimens received and processed in laboratory.
Maintains and updates all laboratory standard operating procedures, policies and procedures and quality management system.
Responsible for ordering supplies and maintaining inventory. Ensure supplies are available as required for lab sessions.
Monitor accrediting agency regulations.
Review Quality Assurance.
Responsible for Employees Performance Appraisals.
Responsible for initial training documentation.
Responsible for ongoing employee competency assessments.
Coordinate on-site training for new and existing staff members.
Ensure communication of laboratory data and appropriate result reporting.
Release samples to laboratory personnel and communicate due dates and update turnaround times.
Ensure compliance with federal, state, and system regulations to provide a safe operation.
Ensure compliance with all corporate policy procedures in the laboratory.
Establish and maintain all laboratory records in accordance with specifications.
Performs other duties as assigned.

CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS

As required by State.

KNOWLEDGE | SKILLS | ABILITIES

Able to deploy dexterity and attention to detail during projects.
A leader, critical thinker, and problem solver.
Knowledge of statistics, spreadsheets, budget planning, cost analysis, and computing.
Collaborate with other team members and clients to solve problems and run programs.
Monitor, analyze and justifies expense and revenue within departments.
Able to handle and the resolution of complex issues and complaints.
Participates in budget planning.
Knowledge in healthcare systems operations.
Knowledge of health care planning and management principles and practices sufficient to manage, direct, and coordinate Care Center operations.
Excellent verbal and written communication skills.
Excellent organizational skills and attention to detail.
Customer-oriented with ability to remain calm in difficult situations.
Delivers exceptional patient service throughout all interactions.
Skill in using computer programs and applications including Microsoft Office.
Ability to build relationships with patients and display empathy and compassion to patients.
Strong analytical and problem-solving skills.
Complies with HIPAA regulations for patient confidentiality.
Complies with all health and safety policies of the organization.

Requirements

EDUCATION REQUIREMENTS

High School Diploma or equivalent required.

Bachelor’s degree in related field strongly preferred.

EXPERIENCE REQUIREMENTS

Minimum 5 years of laboratory experience.

Experience in managing a team of laboratory technicians.

REQUIRED TRAVEL

N/A

PHYSICAL DEMANDS

Carrying Weight

Frequency

1-25 lbs.

Frequent from 34% to 66%

26-50 lbs.

Occasionally from 2% to 33%

Pushing/Pulling

Frequency

1-25 lbs.

Seldom, up to 2%

100 + lbs.

Seldom, up to 2%

Lifting - Height, Weight

Frequency

Floor to Chest, 1 -25 lbs.

Occasional: from 2% to 33%

Floor to Chest, 26-50 lbs.

Seldom: up to 2%

Floor to Waist, 1-25 lbs.

Occasional: from 2% to 33%

Floor to Waist, 26-50 lbs.

Seldom: up to 2%

","hiringOrganization":{"@type":"Organization","name":"AA Urology","sameAs":"https://aaurology.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Annapolis, MD, US","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":40,"item":{"@type":"JobPosting","title":"Laboratory Manager","datePosted":"2025-07-21","description":"

Company Description

Where cutting-edge science meets heartfelt care.

Genea are world leaders in Fertility treatment, we have been providing industry leading success rates for over 35 years and are passionately committed to providing exceptional care to every single patient. With over 50 specialists on our team working Australia wide, Genea is a growing business constantly working to innovate, lift the bar and continually improve outcomes for our patients.

At the core of our business are our people, we work hard to create a workplace that is inclusive, engaging and diverse. Genea is a certified Inclusive Employer (24/25) and Family Friendly Certified workplace, we offer numerous benefits to our staff and truly value the contribution of each individual employee

Job Description

We currently have a great opportunity for a Laboratory Manager to join our Heidelberg team on a full time basis and will consider a Senior Embryologist or experienced leader for this role.

You will be responsible for looking after a small lab and a great team of scientists. As well as participating in the clinical work, you will be responsible for the delivery of the ongoing excellent outcomes that Genea prides itself on. You will have exceptional clinical skills, with the ability to manage complex cases, provide subject matter expertise as well as train and lead a team of Scientists. This role will be varied with many touch points so strength in communications is a must.

Qualifications

We are seeking a skilled and experienced Embryologist or Lab Manager to join our Heidelberg team. This is a fantastic opportunity for someone ready to make a significant impact.

In this role, you will focus on enhancing the patient experience while utilising your strong technical skills to ensure the consistent delivery of exceptional success rates for our patients. We are looking for a strong leader who can head up this small team, someone who can drive engagement and continually develop a team who are eager to learn and grow.

If you are passionate about advancing the field and ready to lead with purpose, we want to hear from you!

Additional Information

Our staff tell us it is the people they work with that makes them stay. That, and our exceptional success rates. It is pretty special working for one of Australia's leading IVF clinics.

And what's in it for you?

We know it's important to look after our staff, so Genea offers a number of perks including;

Glow - Our online recognition and rewards portal. Access discounts at over 350+ retailers as well as accessing recipes, fitness classes and mindfulness sessions
Learning and development – Ongoing opportunities for continuous education through Education Days, internal development, conference opportunities and companywide initiatives
Certified Family Friendly workplace 2024/25

Genea is committed to providing a workplace that is diverse, equitable and inclusive. It is important to us that our hiring process is accessible and open to all, we welcome applications from Indigenous Australians, people with disability, people from diverse cultural and linguistic backgrounds, mature age workers and LGBTIQA+ people.

Please contact our recruitment team (hrrecruit@genea.com.au) if we can help with any reasonable adjustments to enable you to participate in the job application process

","hiringOrganization":{"@type":"Organization","name":"Genea","sameAs":"https://www.genea.com.au"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Heidelberg, VIC, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":41,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-06","description":"

Company Description

SGS is the world leading Testing, Inspection and Certification company. We operate a network of over 2,700 laboratories and business facilities across 119 countries, supported by a team of 99,250 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability.

Job Description

As a Laboratory Technician based in Koolan Island you will be responsible for the quality of preparation and analysis of designated samples during your shift. This is a FIFO positions with a 2&1 roster.

Some other responsibilities include but are not limited to:

Understand the processes of sample preparation and analysis of samples by XRF.
Day to day upkeep of analytical and sample preparation equipment.
Delivery of quality samples to both internal and external customers.
Understand assay methods and recognition of sample types.

Qualifications

The successful person will have:

Experience in a similar laboratory environment.
Experience in sample preparation.
Current drivers licence.
Experience in fusion XRF (desirable).
Laboratory based qualification or similar, in a related field preferred.

Additional Information

WHY WORK FOR SGS?

Working at SGS means joining an innovative, Global company. Here are some of the benefits to working for SGS.

•   As a company, we have embraced the shift to flexible work
\n•   Sustainability is embedded in our culture and the way we do business
\n•   Paid parental leave
\n•   Paid time for volunteering day and blood donations
\n•   Corporate health & wellbeing offers
\n•   Ongoing learning & development
\n•   Career development opportunities (Nationally and Globally)
\n•   SGS Rewards: Our employee benefits platform with access to retail and online discounts and cashback

COME TO WORK AND BE 100% YOU
\n
\nSGS Australia supports a diverse workforce, we encourage applications from people of all ages, nationalities, abilities, and cultures – including Aboriginal and Torres Strait Islander peoples, the LGBTQI+ community and people living with disability. Providing employment opportunities for Aboriginal and Torres Strait Islander people is an important part of our SGS Reconciliation Action Plan (RAP). We truly believe the diversity among us will continue to foster a strong, innovative, and forward-thinking workplace.
\n
\nSGS Australia acknowledges and pays respect to the past, present and future Traditional Custodians and Elders of this nation and the continuation of cultural, spiritual, and educational practices of Aboriginal and Torres Strait Islander peoples.

","hiringOrganization":{"@type":"Organization","name":"SGS","sameAs":"https://sgs.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Koolan Island, WA, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":42,"item":{"@type":"JobPosting","title":"Laboratory Analyst","datePosted":"2025-08-06","description":"

Company Description

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

The Chemical Laboratory Analyst receives sufficient authority from, and is accountable to the respective Department Manager or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position.

The Chemical Laboratory Analyst has authority to identify the occurrence of departures from the quality system or from the procedures for carrying out sample testing, so long as such action does not deviate from established company guidelines, is consistent with sound business or technical judgment, and follows the practices of the laboratory.

OVERALL OBJECTIVES AND RESPONSIBILITIES

Main Assignment

Responsible for all operational activities relative to processing of chemical analytical methods on incoming samples, in compliance with all applicable quality systems.

Care and maintenance of equipment associated with this testing.

Specific Assignments

Perform test methods in accordance with Standard Operating Procedure and applicable Quality Control Procedures

Clean workplace and equipment in accordance with Standard Operating Procedures and general housekeeping requirements.

Maintain and monitor ongoing individual performance of analytical methods with control charts. Notify Department Manager when a batch does not meet batch Quality Control criteria.

Provide feedback to the Department Manager for suggested improvement of analytical methods.

Monitor and meet TAT requirements for sample workflow, and keep the Department Manager informed when capacity constraints are anticipated that may delay TAT.

Record supplies taken from stockroom in logbook, and note any supplies that may need ordering and/or rush delivery.

Maintain assigned equipment and instrumentation according to Standard Operating Procedures. Perform any and all Operational Qualifications prior to analysis according to Standard Operating Procedures.

Qualifications

Bachelor’s degree in chemistry, biology or microbiology, or a high school diploma with the equivalent of 5 years chemical laboratory experience, and basic skills in laboratory techniques.
Willing to work overtime, weekends and holidays
Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Shift: (Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA. are encouraged to apply.

Pay Range: $22/Hr.

Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New Orleans, LA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":43,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-08","description":"

Company Description

Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America.

Job Description

Position Purpose:

Performs a variety of chemical, biological, and physical tests required for research, development or quality control. Compiles data for reports. Responsible for performing routine tasks and analyses on samples in accordance with company and regulatory requirements. May perform specialized analysis under the direction of a Chemist to support applied quality assurance and control procedures. Maintains the laboratory as directed for compliance with company hygiene plans. Assists in special studies in the laboratory and possibly in the field.

Primary Duties /Responsibilities:

Conduct all login procedures, both manual and electronic, of samples delivered to the laboratory, ensuring proper labeling and paperwork.
Sub-sample a variety of materials, process and product samples and follow proper analytical methods required for compliance in accordance with established guidelines and training.
Records and computes results from test data and maintains quality control records and charts as assigned. Performs quantitative and qualitative analyses to determine chemical and physical properties of experimental and developmental materials and may also conduct QA/QC sample analysis and calibrations.
Ensure proper written and electronic documentation of all test results including QA/QC and audits sample documents prior to approval and completeness of summarizing data. Notifies appropriate supervision or staff member of completed analysis.
Prepare reagent/chemical solutions, standards and other laboratory solutions as directed by supervisor or lead technician per guidance and training.
Assists in maintaining an inventory of chemical stores. Collects and logs all Materials Safety Data Sheet (MSDS) documents for chemical stores.
Maintains and distributes as necessary, current Standard Operating Procedures (SOP’s) for applicable methods. Informs Laboratory Supervisory immediately of any personnel, equipment, instrument and material problems and SOP or methodology deviations. Responds to and documents any necessary corrective action.
Perform periodic audits of analytical logs and data to ensure regulatory compliance for completeness and accuracy.
Sets up equipment and instrumentation required for tests, research, or process control. Cleans and makes minor repairs on laboratory apparatus and equipment and ensures a high standard of housekeeping, quality control and safety.
May also label lab waste containers and properly dispose of lab waste per established guidelines.
May assist in other areas or with special projects directed.

Work Environment:

Spends 100% of the time in a lab or operations environment. Typically spends 10 - 20% of time exposed to outdoor and sometimes inclement weather. Company service vehicles are used as required.

Possible Work Hazards:

May be exposed to possible operations hazards including fumes, airborne particles, and noise, rotating machinery, high pressure, hot and cold temperatures, slippery surfaces, water and electrical hazards. Frequently exposed to toxic and caustic chemicals

Physical Demands:

Amount of time spent – Standing 50-75%, Sitting 25%, Walking 25%.
Requires close visual and hearing observation. Taste and smell may be required for some tests.
Constantly uses hands to finger, handle or feel and frequently reaches with hands and arms.
Must be able to lift and carry 50 pounds distances of 10 feet. May lift up to 50-100 pounds on occasion.
Occasional stooping, bending or kneeling, crouching, crawling, climbing, balancing and entering confined spaces.
Close, distance, color and peripheral vision, depth perception and ability to adjust focus are special requirements.

Personal Protective Equipment Required.

Safety Glasses: Continuously

Gloves: Continuously

Hard Hat: Occasionally

Clothing/Coveralls (Tyvek, Poly Coated Tyvek, etc.): Continuously

Hearing Protection: Occasionally

Respirator (Full Face): Frequently

Steel-toed boots: Occasionally

Powered Air Purifying Respirator (PAPR): NA

Apron: Occasionally

Self-Contained Breathing Apparatus (SCBA): NA

Qualifications

Education /Experience /Background:

Associate degree or equivalent, with coursework in qualitative and quantitative Chemistry or biology preferred.
Zero to two years’ experience in a related position in a similar environment with ability to use laboratory apparatus and equipment to perform accurate, repeatable work and to define problems, collect data, establish facts and draw valid conclusions.

Knowledge /Skills /Abilities:

Ability to work with mathematical concepts such as probability and statistical inference and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations.
Ability to interpret a variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Exposure to computerized lab equipment and related systems preferred.
Ability to write reports, business correspondence and procedures manuals.
Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public.
Ability to adhere to Company policies and procedures and to quickly develop proficiency in the care and use of all site specific, facility required PPE (Personal Protection Equipment), including respirators, gas detectors, confined space equipment, etc.)
Must demonstrate ability to work in a team environment and willingness to assume additional or new responsibilities readily.
Excellent interpersonal and communication skills.

Required Certification /Licenses /Training:

Must possess a valid driver’s license and a safe driving record if performing field work.
Employee Orientation, Departmental Operating Procedures, Safety, OSHA and Quality Training.
Learns to perform more complex tests and analysis. Applicable technical training as required.
Stays abreast of new technology, water treatment and separation methods, procedures and regulations infield by reading business periodicals, professional journals, technical procedures and governmental publications.
HAZWOPER (Hazardous Waste Operations and Emergency Response) Level I and II First Responder Certification if required at site.
Must meet minimum qualifications established by regulatory agencies if working in a NELAC or State Certified Lab.
Chemical Hygiene Training.
May perform more advanced functions as part of training and development.

Additional Information

Benefits: Veolia’s comprehensive benefits package includes paid time off policies, as well as health, dental, vision, life insurance, savings accounts, tuition reimbursement, paid volunteering and more. In addition, employees are also entitled to participate in an employer sponsored 401(k) plan, to save for retirement. Pay and benefits for employees represented by a union are outlined in their collective bargaining agreement.

We are an Equal Opportunity Employer! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

","hiringOrganization":{"@type":"Organization","name":"Veolia","sameAs":"https://www.veolia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Port Arthur, TX, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":44,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-04","description":"

What’s the job?

As the Laboratory Technician, you will report to Ashley Hillsley Academic Director-Health and Education and join a passionate team committed to ensuring Torrens University Australia delivers an exceptional student learning experience.

The Laboratory Technician plays a key role in supporting the delivery of high-quality, safe, and engaging learning experiences in specialist teaching laboratories across the Health and Education vertical. Working under the line management of the National Laboratory Manager and day-to-day supervision of a Laboratory Coordinator, the Laboratory Technician operates with a high degree of autonomy and technical expertise in ensuring resource readiness for laboratory classes as part of the laboratory team.

The Laboratory Technician also contributes to the development of operational procedures, supports student learning activities, and provides technical expertise to ensure smooth laboratory operations.

Some delegated responsibilities from the supervising Laboratory coordinator may be assigned based on the needs of the location and the incumbent’s individual skills, expertise and development. These responsibilities may include leading staff training, leading lab projects, providing 2IC cover for lab coordinator.

In this role, you will:

Prepare laboratory environments and equipment in readiness for teaching sessions, simulations, and assessments.

Troubleshoot equipment issues promptly advise laboratory coordinator

Support Laboratory Coordinators in the development and refinement of standard operating procedures.

Assist the National Lab manager and/or the Laboratory Coordinator in daily operations, supporting the team, and potentially making decisions or taking charge of situations in the Laboratory Coordinators absence

Manage the setup and pack down of practical sessions, ensuring all resources and equipment are prepared to specification and stored, recycled or disposed of appropriately after sessions.

Oversee stock usage and advise Laboratory Coordinators on supply levels and reorder requirements.

This is a casual position located at our Brisbane Campus. Availability must include Monday and Friday.

To read more about the role please click here for Job Description.

As this role involves manual handling tasks, the recruitment process will include a functional capability assessment for the preferred candidate. This step aligns with the updated procedures for this position.

Who you are:

To be successful in this role, you will have:

Minimum of a Bachelor qualification in Health Sciences, Biomedical Science, Laboratory Technology, Nursing or a related discipline

2 years experience in a health, clinical, science or educational laboratory environment

Strong analytical and problem-solving skills

Ability to schedule and prioritise effectively

Good communication and interpersonal skills

Ability to work autonomously and with the team

Appropriately qualified in the relevant discipline for level of teaching (qualified to at least one Qualification Standards level higher than the course of study being taught)

We encourage career growth and internal mobility:

As we continue to establish ourselves as a truly global university, we never lose sight of our people-centric approach. Hiring internally, we support professional development, career advancement and personal aspirations to make your working life at Torrens Global Education Services (TUA/Think Education/MDS) a more rewarding experience. Recognising the talent and contributions of our employees, we’ve built a culture that celebrates community, collaboration and innovation, where people love what they do.

Hiring process

We aim to provide you with the necessary information you need at each stage of this process to put your best self forward. Should you have accessibility requirements or needs please contact maur.bell@torrens.edu.au for confidential support to ensure an equitable, barrier free application process as we have a Reasonable Adjustment Procedure in place to support you through the recruitment process.

We are a 2025 Circle Back Initiative Employer and commit to respond to every applicant.

Applications close: Saturday, August 9, 2025

Job reference: R27805

If you require a reasonable accommodation to complete our application process, please contact our Human Resources Department at yourcareer@torrens.edu.au

","hiringOrganization":{"@type":"Organization","name":"Torrens University Australia","sameAs":"https://www.torrens.edu.au/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Campus Brisbane 2, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":45,"item":{"@type":"JobPosting","title":"Laboratory Technician","datePosted":"2025-08-03","description":"

Job Summary

· Assist in the testing of mines samples and assist with the maintenance of equipments.

Key Duties and Responsibilities

· Assist in the analysis of raw materials, intermediate and finished samples.

· Collect samples according to approved quality plan.

· Carry out preliminary preparation of sample collected for X-ray analysis.

· Carry out sieves and moisture analysis of samples.

· Prepare slides and make microscopic observations.

· Ensure cleaning of sample collection points.

· Assist in managing inventory of chemicals and laboratory items including glassware in the laboratory stores.

· Escalate any identified deviations from target quality standards promptly to the supervising Technologist.

· Recommend and implement improvements to the plant’s laboratory operations and maintenance of lab equipments and instruments.

· Ensure effective house-keeping in the laboratory.

· Assist in the maintenance of ISO quality management systems in the unit.

· Assist in the preparation of periodic lab analysis and activity reports.

· Perform any other duties as assigned by the Head, Quality Control & Assurance or relevant supervising Officer.

Requirements

Key Requirements

Education and Work Experience

· High National Diploma (HND) or its equivalent in any discipline.

· Minimum of two (2) years relevant work experience.

Skills and Competencies

· Good problem solving and analytical skills

· Good knowledge of laboratory terminology and equipments

· Ability to handle samples and operate lab equipments

· Ability to pay attention to details

· Good communication skills

· Proficiency in Microsoft Office Suites

Benefits

Private Health Insurance

Paid time off

Learning & Development

","hiringOrganization":{"@type":"Organization","name":"Dangote Group","sameAs":"https://www.dangote.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Douala, Littoral Region, Cameroon","addressCountry":"Cameroon","addressRegion":"Africa"}}}},{"@type":"ListItem","position":46,"item":{"@type":"JobPosting","title":"Laboratory Analyst","datePosted":"2025-08-04","description":"

Company Description

Job Description

Eurofins Built Environment Testing is proactively seeking an analyst to join our Naperville site.

The Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation.

Analyst responsibilities include, but are not limited to, the following:

Prepare and analyze environmental samples
Accurately enters and reports analytical data using the LIMS
Performs independent data reviews for other analysts’ work
Performs analysis of reference materials, proficiency samples and other quality control samples as needed
Maintains client service and provides technical support as needed
Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests
Performs confirmation of lab results as needed by client services personnel
Performs and completes all analytical testing QA related tasks as needed
Assists in pursuing, receiving and maintaining necessary laboratory accreditations
Maintains and updates all necessary Training and QA documents onsite as necessary
Co-ordinates and manages projects according to their rush status and due time for timely delivery
Assists co-workers on analytical questions, as necessary
Participates in Lean initiatives and projects when called upon
Follows company policies and procedures
Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed
Manages and disposes analyzed samples as needed
Trains new mycology, asbestos or geology analytical testing analysts as needed
Recommends and coordinates sample transfer as necessary
Establishes and maintains laboratory stock culture and reference samples
Performs root cause analysis and determines and implements corrective actions for errors and issues as necessary
Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed
Routinely communicates available capacity to Regional Manager
Other responsibilities as deemed necessary by the Supervisor/Manager

Qualifications

Qualifications

Basic Minimum Qualifications:

BS or BA in a closely related science
1- 2 years of previous experience with Asbestos, Mycology, Forensic Sciences or Geology testing services within a laboratory setting.
Professional working proficiency in English is a requirement, including the ability to read, write and speak in English
Authorization to work in the United States indefinitely without restriction or sponsorship

The ideal candidate would possess:

Environmental methodologies within Asbestos, Mycology, Forsensic Science or Geology
General regulatory requirements
Analytical laboratory techniques
Laboratory QA requirements
Knowledge of computers, spreadsheets, and databases
Strong computer, scientific, and organizational skills

Additional Information

Position Pay Range starts at $17.75/hr based on experience

Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business section, and geographic location

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

Find out more in our career page: https://careers.eurofins.com/

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
\n
\nEurofins Environment Testing Businesses in the US are routinely engaged in Federal Contracts. Federal Government vaccination mandates may apply to staff working in these businesses. Successful applicants may be required to confirm vaccination status or demonstrate eligibility for medical or religious exemptions prior to commencing employment. In addition, certain positions require travel for which vaccination is required in accordance with Eurofins policy.

Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Naperville, IL, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":47,"item":{"@type":"JobPosting","title":"Laboratory Analyst","datePosted":"2025-08-07","description":"

Company Description

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

OVERALL OBJECTIVES AND RESPONSIBILITIES

Main Assignment

Responsible for all operational activities relative to processing of chemical analytical methods on incoming samples, in compliance with all applicable quality systems.

Care and maintenance of equipment associated with this testing.

Specific Assignments

Perform test methods in accordance with Standard Operating Procedure and applicable Quality Control Procedures

Clean workplace and equipment in accordance with Standard Operating Procedures and general housekeeping requirements.

Maintain and monitor ongoing individual performance of analytical methods with control charts. Notify Department Manager when a batch does not meet batch Quality Control criteria.

Provide feedback to the Department Manager for suggested improvement of analytical methods.

Monitor and meet TAT requirements for sample workflow, and keep the Department Manager informed when capacity constraints are anticipated that may delay TAT.

Record supplies taken from stockroom in logbook, and note any supplies that may need ordering and/or rush delivery.

Qualifications

Bachelor’s degree in chemistry, biology or microbiology, or a high school diploma with the equivalent of 5 years chemical laboratory experience, and basic skills in laboratory techniques.
Willing to work overtime, weekends and holidays
Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Shift: (Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA. are encouraged to apply.

Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

","hiringOrganization":{"@type":"Organization","name":"Eurofins","sameAs":"https://www.eurofins.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New Orleans, LA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":48,"item":{"@type":"JobPosting","title":"Laboratory Assistant","datePosted":"2025-08-07","description":"

How Corewell Health cares for you

Comprehensive benefits package to meet your financial, health, and work/life balance goals. Learn more here.
On-demand pay program powered by Payactiv
Discounts directory with deals on the things that matter to you, like restaurants, phone plans, spas, and more!
Optional identity theft protection, home and auto insurance, pet insurance
Traditional and Roth retirement options with service contribution and match savings
Eligibility for benefits is determined by employment type and status

Primary Location

SITE - Royal Oak Hospital - 3601 W 13 Mile Road - Royal Oak

Department Name

Lab - Clinical Pathology Blood Bank - CH East - North - Royal Oak

Employment Type

Full time

Shift

Day (United States of America)

Weekly Scheduled Hours

Hours of Work

7:00am-3:30 pm

Days Worked

Monday-Friday

Weekend Frequency

N/A

CURRENT COREWELL HEALTH TEAM MEMBERS – Please apply through Find Jobs from your Workday team member account. This career site is for Non-Corewell Health team members only.

Corewell Health is committed to providing a safe environment for our team members, patients, visitors, and community. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category. We are committed to supporting prospective team members who require reasonable accommodations to participate in the job application process, to perform the essential functions of a job, or to enjoy equal benefits and privileges of employment due to a disability, pregnancy, or sincerely held religious belief.

Corewell Health grants equal employment opportunity to all qualified persons without regard to race, color, national origin, sex, disability, age, religion, genetic information, marital status, height, weight, gender, pregnancy, sexual orientation, gender identity or expression, veteran status, or any other legally protected category.

An interconnected, collaborative culture where all are encouraged to bring their whole selves to work, is vital to the health of our organization. As a health system, we advocate for equity as we care for our patients, our communities, and each other. From workshops that develop cultural intelligence, to our inclusion resource groups for people to find community and empowerment at work, we are dedicated to ongoing resources that advance our values of diversity, equity, and inclusion in all that we do. We invite those that share in our commitment to join our team.

You may request assistance in completing the application process by calling 616.486.7447.

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Company :

Hastings Deering (Australia) Ltd

About the Role

Are you ready to dive into a world of innovation and opportunity? Hastings Deering is now on the lookout for motivated individuals to join our world-class laboratory as Trainees!

Gain real, hands-on experience, receive top-tier on-the-job training, and best of all — walk away with a Certificate III in Laboratory Skills to launch your career in style! This is a 2 year contract with a possibility for a full time role at the end!

In this position, you will:

Collection of samples from designated collection points within the premises
Unpacking and sorting samples
Assigning label numbers appropriately
Analysis of routine samples as designated using various instrumentation
Correlation of data
Competency based laboratory studies
Housekeeping and general equipment maintenance
Preparation of laboratory standards
Calibration of instrumentation
Display care in the use of company instrumentation, tools and property

Why Hastings Deering?

At Hastings Deering, our people are our heart – from their first day with us right up to their last.

As one of the top Caterpillar dealers globally and part of the Sime Darby network, you’ll have access to extensive and borderless career development opportunities and enjoy an internationally recognised work culture.

Whether you’re looking to take your career to the next level or achieve more balance in your schedule, we offer diverse opportunities for talented professionals to join our team and start something big.

You’ll have access to:

Opportunities for training, mentorship, and career development specific to your role.
Competitive remuneration package and annual salary reviews
A supportive, diverse, and inclusive team spread across Australia and internationally.
Access to growth opportunities at a regional, national, and international level through our global Sime Darby network.
Dedicated programs and utilities to support your physical, mental, and financial health, such as our Employee Assistance Program, free health checks, and discounted private health insurance.
Employee discounts, rewards, and incentive programs.
Salary continuance insurance

About You

Hold a year 12 certificate
You must not hold a qualification higher than a Certificate III in Laboratory Skills or you are not eligible (ie, a science degree or a cert IV in Laboratory Skills)
Willingness to learn
Based in SEQ at the time of application
Interest in pursuing a career in a laboratory environment
Australian Citizen or Permanent Resident (we are unable to accept applications from candidates who are temporary residents)

To Apply: Hit the ‘Apply Now’ button

Enquiries: Please call 1300 071 618

Contact Person: Brianna Smith – Brianna.l.smith@hastingsdeering.com.au

About Hastings Deering

Hastings Deering is one of the top 5 Caterpillar dealerships globally. We sell, rent, and offer support and parts distribution services for Cat® products across a range of industries, including resources, general construction, civil transport and commercial construction, power systems, government, primary industries and marine.

We have more than 3,500 employees across 23 business service centres throughout Queensland, Northern Territory, Papua New Guinea, the Solomon Islands and New Caledonia, with our headquarters based in Brisbane, Australia.

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Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

Supervises the day-to-day operation of the department to ensure smooth flow of samples and testing
Oversees the scheduling of staff to ensure production schedules are met
Counsels staff with regard to problems encountered in daily operations
Identifies process improvements to better meet client expectations and company objectives
Recommends new equipment for the department
Oversees the monitoring of inventory/ordering by establishing and maintaining par levels and re-stocking points for supplies and reagents
Serves as a liaison for the department to outside vendors
Supports Eurofins DPT’s business philosophy, leadership values and ethics
Conducts timely investigations in coordination with Quality Assurance related to site quality events, including but not limited to customer complaints, inquiries, non-conformances, corrective actions, and audit findings
Works with Quality Assurance to resolve client complaints by investigating problems, developing solutions, and making recommendation to management
Performs duties in compliance with all applicable regulatory and accrediting agencies and cGMP expectations, including, but not limited to: facility and equipment maintenance, validation review and approval, and training (internal, continuing education, proficiency testing, annual cGMP, etc.)
Meets basic expectations of DPT’s quality management system, including but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, and accurate recordkeeping so the company may meet its stated quality policy and objectives
Agrees to be accessible (by telephone or synchronous two-way electronic audio-visual communication) to testing personnel during times when testing is performed. (Note: The accessibility to testing personnel may be shared among other supervisory staff, appropriate management, and/or Laboratory Directors.)

The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Qualifications

MINIMUM EDUCATIONAL REQUIREMENTS

Bachelor’s degree in Chemical, Physical, or Biological Science or Laboratory Science required.

In addition:

DPT San Ramon labs: licensure by the State of California Department of Public Health as a Clinical Laboratory Scientist.
For DPT Honolulu lab: licensure by the State of Hawaii Department of Health for the specific laboratory testing being supervised.

WORK EXPERIENCE REQUIREMENTS

Meet the minimum, applicable work experience to work in a CMS CLIA designated high-complexity laboratory per 42 CFR Part §493.1461.
If Laboratory is CAP or ASHI Accredited, three (3) years of Histocompatibility/Immunogenetics experience is needed to supervise Histocompatibility/Immunogenetics testing per ASHI Standard E.5 and/or CAP HSC.46250.
Considerable knowledge of the methods, materials, and techniques used in laboratory testing
Considerable knowledge of the use of laboratory apparatus and equipment
Ability to organize, communicate, teach, and work with others in an effective manner
Ability to manage and schedule the work of others
Knowledge of federal, state, and local standards, regulations, guidelines, and requirements affecting operations of a clinical reference laboratory
Analytical thinking and communication skills

POTENTIAL ENVIRONMENTAL FACTORS

This laboratory carefully maintains all hazardous materials. All employees must abide by Eurofins DPT’s Safety and Exposure procedures. This includes using the provided safety clothing and equipment.
For a list of potential chemical hazards, see appropriate MSDS sheet.

Additional Information

Compensation:

$90,000 - $110,000

Schedule:

Monday-Friday 8:00am-5:00pm

What we offer:

Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

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