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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Quality

Job Sub Function:

Quality Systems

Job Category:

Professional

All Job Posting Locations:

Beerse, Antwerp, Belgium, Gent, East Flanders, Belgium

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Quality Systems Associate CAR-T to be in Ghent, Belgium!

Purpose: CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, Janssen is building two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories will be operated from the existing Janssen Beerse site.

In this role you will be responsible for management and monitoring of the quality systems processes supporting the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.

As a Quality Systems Associate, you will:

Own or support QSEs such as Event Management, Change Control, and Supplier Management for Carvykti.
Develop and document QSE processes in procedures and work instructions.
Act as site expert and trainer for QSE-related topics.
Conduct gap assessments and ensure process compliance.
Monitor and improve QSE performance across the CAR-T organization.
Serve as Trackwise/COMET key user: manage access, train users, and represent the site in global forums.
Ensure inspection readiness and alignment with J&J policies, cGMP, and quality standards.
Identify and implement process improvements to support Carvykti’s success.

Qualifications/Requirements:

Graduate degree or higher in Science, Bioengineering, pharmacy or related field, or equal by experience
Strong understanding of the pharmaceutical environment, regulatory requirements and cGMP
Knowledge of the different quality processes and quality systems
Knowledge to perform investigations and risk analyses
Communicative skills to collaborate with different business partners (both Dutch and English)
You have a quality mentality
You are flexible to support shifting priorities
You continuously look for improvements

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here’s what you can expect:

Application review: We’ll carefully review your CV to see how your skills and experience align with the role.

Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.

Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.

Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.

Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA

","hiringOrganization":{"@type":"Organization","name":"Johnson & Johnson","sameAs":"https://www.jnj.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"BE022 GENT, Belgium","addressCountry":"Belgium","addressRegion":"Europe"}}}},{"@type":"ListItem","position":2,"item":{"@type":"JobPosting","title":"Associate, Quality Systems","datePosted":"2025-09-10","description":"

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

The Quality Systems Associate will provide Quality Systems support to UK and Ireland Compounding organization to ensure that all sites maintain a compliant, efficient Quality Management System (QMS) in accordance with local regulatory requirements for Good Manufacturing Practice and Baxter Global QMS requirements and to manage and act as SME for the Documentation Control process.

Reports into the UK Compounding Quality System Manager.

Essential Duties And Responsibilities:

Responsible for the effective management of the UKI Documentation Control process, in compliance with Global and local Regulatory requirements, by quality data monitoring and analysis
Coordinate the content review of the Global Quality Documents in draft stage and the implementation assessment of Global Quality Documents issued with SMEs.
Execute documentation reviews as required
Act as Subject Matter Expert for the Documentation Control process (TcU author and Change Specialist 3) & archiving
Provides Training support as an SME in documentation control and archiving
Support the trending, monitoring and reporting of NCR/CAPA/CQI/CPI in TW8 to facilitate Quality Management Review (QMR).
Support Internal, Corporate, external Regulatory and Customer audits through provision of requested documentation, records and information in a timely manner
Other duties in support of Compounding Quality Systems as required, including support to Regional/Global Compounding

Experience and Qualifications:

Eligibility required: Resident and eligible to work in the UK on a full-time basis.

English minimum equivalent to RQF Grade 2, EQF Grade 3 or SCQF Grade 5
At least 2 years’ experience in the pharmaceutical or medical device industry.
Experience working in a Quality function
Experience of Baxter systems and processes.
Bachelor’s degree or higher in Pharmacy, or other relevant scientific discipline, such as chemistry
Experience in implementing and maintaining quality systems in a regulated environment, including document control, change control, nonconformance management, validation.
High level of proficiency in IT systems and data analysis and visualization applications
Experience with other IT systems is advantageous.

What are some of the benefits of working at Baxter?

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Commitment to growing and developing an inclusive and diverse workforce

#LI-MT1

#IND-UKOPS

#IND-UKCOM

#LI-BAXGEN

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

","hiringOrganization":{"@type":"Organization","name":"Baxter International Inc.","sameAs":"https://www.baxter.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"UCROY - UK - Croydon, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":3,"item":{"@type":"JobPosting","title":"Associate Quality Systems Specialist","datePosted":"2025-09-03","description":"We anticipate the application window for this opening will close on - 12 Sep 2025

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Medtronic is hiring in Woolwich County, here our employees are helping us deliver on the extraordinary. We actively seek a diverse workforce at every level: We require fresh ideas and inclusive insights to maintain our position as an innovative industry leader. That’s why we actively seek, attract, and develop employees who are patient-centric, passionate, and who reflect the wide variety of life experiences found among our patients.
We’ve been on a three-year journey to modernize our U.S. distribution network and transform how we distribute our products. The Woolwich Distribution site is one of two new U.S. distribution hubs opened within the last year to enhance and streamline our delivery operations. We’re aiming to elevate the customer experience and generate cost savings with state-of-the-art technology and standardized processes. But none of it can happen without you – the people who power our operations and ensure that our customers receive our life-saving therapies when they need them.

Responsibilities may include the following and other duties may be assigned.

Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
Prepares reports and/or necessary documentation (ex Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.
Co-ordinates legal requests in support of government investigations or litigations.
Ensures the quality assurance programs and policies are maintained and modified regularly.
Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.

Required Knowledge and Experience:
Requires a Baccalaureate degree

Preferred Qualifications:

Knowledge and experience with CAPA, Audits, Quality Audits, QMS structure
,Knowledge of ISO 14385 and 21 CFR 820
Quality Management or Document Control experience

Experience with TrackWise
Certified Auditor
Working knowledge of Microsoft Office tools, desktop publishing software experience (Microsoft Office Suite, Adobe Acrobat)

Familiar with modern ERP (Enterprise Resource Planning) systems, PLM (Product Lifecycle Management) systems and manufacturing documentation (i.e. BOMs, item masters, DHF, DMR, etc.)

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):59,200.00 - 88,800.00

The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here.

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

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A Day in the Life

Medtronic is a market leader, and our expanding portfolio delivers measurable clinical and economic value – and opens doors. With a passion for helping patients and a commercial mindset, you will make a significant difference together with Medtronic!

The Associate Quality Systems Specialist will handle the PMV operations to ensure the company is operating and meeting the established quality standard of medical devices across all business. This is a rare and incredible opportunity to enhance your skillset in supporting our market leading technology across a broad range of products.

Responsibilities may include the following and other duties may be assigned:

Ensure that Medtronic Korea is complaint with Korea medical device regulation and ISO 13485
Maintain QMS procedures and quality records to align with global policies, local regulation, and local practice
Establish training matrix and assign training in learning management system
Conduct internal audit and corrective and preventive actions
Support external audit (e.g., MFDS’s random product inspection, unannounced surveillance inspection, foreign material event inspection, etc.)
Manage distributors and suppliers
Manage change control and risk management
Handle Product Complaint
Handle vigilance reporting (incl. overseas adverse event) and foreign material event reporting
Execute Field Corrective Action (FCA)
Implement Enterprise and regional projects for continuous improvement
Obtain KGMP certificate for overseas manufacturing sites

Required Knowledge and Experience:

Bachelor’s degree required in medical, biological science or equivalent field
Prior experience in a Quality Specialist role is essential with 1 to 2 years of relevant experience, preferably medical devices.
Effective written and verbal communication skills in English and Korean languages
Strong ability to work well within a team and autonomously
Achievement oriented and ability to drive results with the highest quality standards
Computer skills (excellent knowledge of MS Office products)
High attention to detail and accuracy
Good prioritization and organizational skills
Excellent problem-solving skills

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

Benefits & Compensation

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

Learn more about our business, mission, and our commitment to diversity here

","hiringOrganization":{"@type":"Organization","name":"Medtronic","sameAs":"https://www.medtronic.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"KOR-11 Seoul, Korea, Republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":5,"item":{"@type":"JobPosting","title":"Associate Quality Systems Specialist","datePosted":"2025-09-10","description":"

A Day in the Life

Responsibilities may include the following and other duties may be assigned:

Ensure that Medtronic Korea is complaint with Korea medical device regulation and ISO 13485
Maintain QMS procedures and quality records to align with global policies, local regulation, and local practice
Establish training matrix and assign training in learning management system
Conduct internal audit and corrective and preventive actions
Support external audit (e.g., MFDS’s random product inspection, unannounced surveillance inspection, foreign material event inspection, etc.)
Manage distributors and suppliers
Manage change control and risk management
Handle Product Complaint
Handle vigilance reporting (incl. overseas adverse event) and foreign material event reporting
Execute Field Corrective Action (FCA)
Implement Enterprise and regional projects for continuous improvement
Obtain KGMP certificate for overseas manufacturing sites

Required Knowledge and Experience:

Bachelor’s degree required in medical, biological science or equivalent field
Prior experience in a Quality Specialist role is essential with 1 to 2 years of relevant experience, preferably medical devices.
Effective written and verbal communication skills in English and Korean languages
Strong ability to work well within a team and autonomously
Achievement oriented and ability to drive results with the highest quality standards
Computer skills (excellent knowledge of MS Office products)
High attention to detail and accuracy
Good prioritization and organizational skills
Excellent problem-solving skills

Benefits & Compensation

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

Learn more about our business, mission, and our commitment to diversity here

","hiringOrganization":{"@type":"Organization","name":"Medtronic","sameAs":"https://www.medtronic.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"KOR-11 Seoul, Korea, Republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":6,"item":{"@type":"JobPosting","title":"Associate Quality Systems Specialist","datePosted":"2025-09-10","description":"

A Day in the Life

Responsibilities may include the following and other duties may be assigned:

Ensure that Medtronic Korea is complaint with Korea medical device regulation and ISO 13485
Maintain QMS procedures and quality records to align with global policies, local regulation, and local practice
Establish training matrix and assign training in learning management system
Conduct internal audit and corrective and preventive actions
Support external audit (e.g., MFDS’s random product inspection, unannounced surveillance inspection, foreign material event inspection, etc.)
Manage distributors and suppliers
Manage change control and risk management
Handle Product Complaint
Handle vigilance reporting (incl. overseas adverse event) and foreign material event reporting
Execute Field Corrective Action (FCA)
Implement Enterprise and regional projects for continuous improvement
Obtain KGMP certificate for overseas manufacturing sites

Required Knowledge and Experience:

Bachelor’s degree required in medical, biological science or equivalent field
Prior experience in a Quality Specialist role is essential with 1 to 2 years of relevant experience, preferably medical devices.
Effective written and verbal communication skills in English and Korean languages
Strong ability to work well within a team and autonomously
Achievement oriented and ability to drive results with the highest quality standards
Computer skills (excellent knowledge of MS Office products)
High attention to detail and accuracy
Good prioritization and organizational skills
Excellent problem-solving skills

Benefits & Compensation

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

Learn more about our business, mission, and our commitment to diversity here

","hiringOrganization":{"@type":"Organization","name":"Medtronic","sameAs":"https://www.medtronic.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"KOR-11 Seoul, Korea, Republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":7,"item":{"@type":"JobPosting","title":"Associate Quality Systems Specialist","datePosted":"2025-09-10","description":"

A Day in the Life

Responsibilities may include the following and other duties may be assigned:

Ensure that Medtronic Korea is complaint with Korea medical device regulation and ISO 13485
Maintain QMS procedures and quality records to align with global policies, local regulation, and local practice
Establish training matrix and assign training in learning management system
Conduct internal audit and corrective and preventive actions
Support external audit (e.g., MFDS’s random product inspection, unannounced surveillance inspection, foreign material event inspection, etc.)
Manage distributors and suppliers
Manage change control and risk management
Handle Product Complaint
Handle vigilance reporting (incl. overseas adverse event) and foreign material event reporting
Execute Field Corrective Action (FCA)
Implement Enterprise and regional projects for continuous improvement
Obtain KGMP certificate for overseas manufacturing sites

Required Knowledge and Experience:

Bachelor’s degree required in medical, biological science or equivalent field
Prior experience in a Quality Specialist role is essential with 1 to 2 years of relevant experience, preferably medical devices.
Effective written and verbal communication skills in English and Korean languages
Strong ability to work well within a team and autonomously
Achievement oriented and ability to drive results with the highest quality standards
Computer skills (excellent knowledge of MS Office products)
High attention to detail and accuracy
Good prioritization and organizational skills
Excellent problem-solving skills

Benefits & Compensation

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

Learn more about our business, mission, and our commitment to diversity here

","hiringOrganization":{"@type":"Organization","name":"Medtronic","sameAs":"https://www.medtronic.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"KOR-11 Seoul, Korea, Republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":8,"item":{"@type":"JobPosting","title":"Associate - PR&D Quality Systems","datePosted":"2025-07-21","description":"

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Organization Overview:

The PR&D Quality Systems (QS) Team is responsible for the overall strategic leadership and management of the PR&D Quality System (QS), including the business processes that support PR&D QS documents. As part of this team, the Manager is responsible for overseeing the review, approval, and maintenance of QS documents, partnering with key business areas, and ensuring the integrity of the PR&D QS.

Responsibilities:

PR&D QS Management

Manage PR&D QS documents through preparation, review, approval, and maintenance processes to meet business and compliance needs.
Oversee the periodic review process to ensure compliance requirements and timelines are met.
Maintain the integrity of the Quality System Index.
Apply knowledge of current business, regulatory, industry, and overarching requirements to uphold the quality of all documents and the integrity of the PR&D QS.
Ensure accurate and timely implementation of deliverables/documents.

Customer Interaction & Influence

Support stakeholders and teams with expertise in PR&D QS and document management processes.
Guide Document Owners, Reviewers, and Approvers by communicating key process expectations.
Collaborate with Learning & Development to drive action and ensure process requirements and deadlines are met.
Build, maintain, and leverage relationships with customers and business partners to achieve results.
Anticipate customer needs and provide proactive support.

Process Leadership and Improvement

Own, manage, and lead key Standards Team processes to ensure ongoing compliance and audit readiness.
Identify and implement improvements to business processes supporting the PR&D QS.
Participate in and contribute to project initiatives.
Leverage technical expertise to influence key process decisions.

Basic Requirements:

Bachelor of Science in applicable field
2+ years of experience working with quality
Experience with Document Management Systems and processes (Veeva Vault)

Additional Skills/Preferences:

In-depth knowledge of GXPs.
Familiarity with Operational Excellence principles.
Understanding of Risk Management principles.
Technical writing experience.
Strong project management, communication, and problem-solving skills.
Advanced computer skills (Microsoft Office).
Demonstrated collaboration to meet shared goals.

Additional Information:

On Site Expectations: minimum of 3 days on site

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$63,000 - $140,800

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

","hiringOrganization":{"@type":"Organization","name":"Eli Lilly and Company","sameAs":"https://www.lilly.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US: Indianapolis IN Tech Center North, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":9,"item":{"@type":"JobPosting","title":"Senior QA Associate – Quality Systems","datePosted":"2025-08-25","description":"

Job Function:

Quality

Job Sub Function:

Quality Systems

Job Category:

Professional

All Job Posting Locations:

Geel, Antwerp, Belgium

Job Description:

Within J&J Innovative Medicine Supply Chain, a member of Johnson & Johnson's Family of Companies, we are recruiting a Senior QA Associate – Quality Systems (M/F/X).

As a member of our Quality team overseeing the Quality Systems (QS) processes, you will be based in Geel, Belgium.

J&J Innovative Medicine Supply Chain Geel serves as Center of Excellence for the development and manufacturing of Small Molecule API (SM-API) and DP Intermediates used in treatments that improve the health and lifestyle of people worldwide. J&J Innovative Medicine Supply Chain Quality supports the Geel site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of SM-API and DP Intermediates, guaranteeing reliable supplies in compliance with applicable regulations.

As Senior QA Associate – Quality Systems, you are Subject Matter Expert of Quality System processes such as document management, records management. You drive the implementation at the Geel site and ensure adherence to the Quality System. In this role you report directly to the Senior QA Manager.

In this role you are responsible to:

Establish and maintain strong working relationships with your global Quality Systems partners as well as your local Quality and Supply Chain colleagues
Act as QA Point of Contact for the Geel site ensuring Quality Systems are appropriately implemented and applied in compliance with global regulations and J&J quality requirements
Coach cross-functional teams at the site, including Quality professionals
Act as Local Process Owner for Quality System processes such as document management, records management,… by:
- Acting as local Subject Matter Expert, ensuring GMP documentation is in place and training provided in compliance with global regulations and J&J quality requirements
- Providing support to local users and QA approvers
- Driving the site to continuously strengthen related skill sets across the entire organization
- Evaluating trends and defining appropriate actions
- Defining, following up and concluding corrective and preventive actions related to the Quality System processes
Ensure that quality records such as change controls, non-conformances and CAPAs are handled properly and in a timely manner by providing quality, compliance and technical expertise so that the internal and external customer expectations are met
With focus on Quality Systems processes, develop and foster an environment of innovative thinking through e.g. benchmarking and training. Continuously challenge the status quo by identifying opportunities for continuous improvement
Lead and participate in continuous improvement initiatives on the Quality System processes
Act as spokesperson during Health Authority inspections and customer audits

Qualifications:

Master Scientific degree with a technical specialization in analytics / chemistry / biotechnology / pharmaceutical sciences (or equivalent through experience)
In-depth knowledge of cGMP (domestic & international), ICH guidelines, policies, standards and procedures
Experience in Chemical and/or Pharmaceutical Quality Control and/or Quality Assurance
Experience with Data Analysis and continuous improvement methodologies is an asset
Experience in people leadership is an asset
You work accurately and proactively seek solutions
You have good communication skills
You speak and write Dutch and English fluently
Strong analytical thinking skills and the ability to work in a flexible way under time pressure in local and global teams. Ability to make risk based decisions under time pressure. Understands the business implications regarding quality positions and decisions.

","hiringOrganization":{"@type":"Organization","name":"Johnson & Johnson","sameAs":"https://www.jnj.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"BE006 Geel, Belgium","addressCountry":"Belgium","addressRegion":"Europe"}}}},{"@type":"ListItem","position":10,"item":{"@type":"JobPosting","title":"Senior Quality Systems Engineer/ Quality Systems Engineer","datePosted":"2025-09-11","description":"

About The Role

Our strong focus on research and development creates a regular flow of new Fisher & Paykel Healthcare products. To enable our ongoing success, we depend on the technical expertise of our Design Assurance team who ensure our products get to market as fast as possible while meeting customer, business and international regulatory requirements.

Non Invasive Ventilation Team is set to be a strong long-term focus for FPH, and with a vast range of new and existing NIV products, it’s an exciting area to be a part of.

In this role supporting our NIV Team, you will act as a technical subject matter expert in engineering and quality systems to drive quality improvements. You will provide training, development and expert advice to support the achievement of the Respiratory Humidification (RH) product group’s business plan and ensure compliance to the QMS and regulatory requirements, improving our ability to meet market expectations.

About You

We are looking for someone with:

5+ years related experience in the medical device industry, ideally with experience across multiple roles.
A tertiary degree in Science or Engineering.
Comprehensive knowledge of medical device processes and relevant industry standards.
Technical specialist knowledge of FPH products and business.
A holistic approach to product development.

You will also have:

Excellent communication skills with the ability to influence, negotiate and challenge with respect and diplomacy.
A curious and inquisitive nature and a continuous improvement mindset.
An ability to build relationships at all levels within the organization.

Depending on the experience of the candidate, we have the flexibility to consider candidates at the Quality Systems Engineer level as well as Senior Quality Systems Engineer level.

Working With Us

Care to join a supportive environment? Fisher & Paykel Healthcare foster an inclusive work environment founded on our culture of care and cooperation. Here you’ll have the trust and support to generate ideas, solve problems and do your best work, while enjoying some of our perks and benefits:

Employee share purchase scheme
Discretionary bi-annual Profit share
Generous Paid Parental Leave
Life, Critical illness and Income Protection Insurance
Discounted Health Insurance
Active Social clubs & community groups
In-house training programs from external providers
Purchasing privileges for Fisher & Paykel Healthcare
School holiday programme subsidy
Banking and Insurance discounts
Free Parking
Beautiful campus with green spaces
Subsidised Café’s
Annual Salary Review
High rates of internal promotion

Access to state-of-the-art facilities

About Us

Fisher & Paykel Healthcare is a world leader in the design, manufacture, and marketing of medical devices, exporting to over 120 countries globally.

Our commitment to care unites us. Here, we’re driven to improve patient care and outcomes through inspired and world-leading healthcare solutions.

Care to join us? Apply today

This is an exciting opportunity to leverage your relationship and engagement skills to partner across the business and externally (such as with academics and medical professionals, and other outside organisations).

We focus on nurturing a positive and inclusive culture based on trust and respect. In New Zealand, our employee-led communities, Spectra (rainbow), Manaaki (Māori) and Women in Engineering play an important role in this culture. We also have a commitment to creating a positive lasting impact on society, shown by our support of New Zealand organizations such as Te Uru Tangata – Centre for Workplace Inclusion, Pride Pledge and Global Women.

We are dedicated to designing our recruitment process with care and empathy to support all candidates, regardless of identity, background, and experiences. Should you require support or adjustments during our process, please let us know at recruit@fphcare.co.nz.

Requisition ID: 5926
\nPosting end date: 25/09/2025

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A Day in the Life

Responsible for overseeing and maintaining the quality management systems (QMS). This role ensures that all processes and products comply with regulatory standards and internal quality requirements.
Develop, implement, and maintain the QMS in accordance with applicable regulations.
Ensure continuous improvement of quality processes.
Oversee documentation processes to ensure accuracy and completeness.
Maintain records of quality metrics and performance indicators.
Foster a culture of quality awareness across the organization.
Facilitate communication between teams to resolve quality-related issues.

Responsibilities may include the following and other duties may be assigned.

Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
Prepares reports and/or necessary documentation (ex Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.
Co-ordinates legal requests in support of government investigations or litigations.
Ensures the quality assurance programs and policies are maintained and modified regularly.
Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.

PEOPLE MANAGEMENT FUNCTIONAL CAREER STREAM: Management and supervisory professionals with one or more employees who are focused on tactical, operational and some strategic activities within a specified area. Levels within the management career stream typically have six or more direct reports. The majority of time is spent overseeing their area of responsibility, managing performance, developing talent, engagement and inclusion, communicating business and operational developments, planning, prioritizing and / or directing the responsibilities of direct reports. Goal achievement is typically accomplished through performance of direct and / or indirect reports. A key responsibility of roles in this career stream is managing people. which includes: accountability for mentoring, developing and coaching staff on meeting/exceeding performance expectations and defined objectives, providing leadership to staff ensuring the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.

DIFFERENTIATING FACTORS

Autonomy: Manages subordinate supervisors and/or experienced professionals who exercise latitude and independence in assignments.
Provides tactical and / or operational leadership and coaching.
Receives assignments in task and objective oriented terms.

Organizational Impact: Establishes operational plans and implements policies and strategies.
Decisions impact program schedules, customer satisfaction levels, or allocation of time, material resources, expenditures and funds.
May have budget or P&L accountability for a department, function or geography.
Strive for continuous improvement and consistency in deliverables.

Innovation and Complexity: Proposes modifications to functional operating policies and day-to-day processes.
Problems and issues faced are complex, difficult and undefined, and require detailed information gathering, analysis and investigation to understand the problem.

Communication and Influence: Communicates with internal and external customers and vendors regarding ongoing operations.
Uses information exchange, influence and active persuasion without direct exercise of command to gain cooperation of other parties .
May interact on issues that have externally shared objectives.

Leadership and Talent Management: Manages a team consisting of supervisors and / or experienced professionals in the Specialist career stream.
Leads, directs and reviews the work of a team who exercise latitude and independence in their assignments.
Authorizes hiring, firing, promotion and reward within own area.

Required Knowledge and Experience: Requires practical knowledge in leading and managing the execution of processes, projects and tactics within one job area.
Typically has advanced knowledge and skills within a specific technical or professional discipline with understanding of the impact of work on other areas of the organization.
Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) and minimum of 5 years relevant experience, or advanced degree with a minimum of 3 years prior relevant experience.

Benefits & Compensation

About Medtronic

Learn more about our business, mission, and our commitment to diversity here

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Quality Management is responsible for ensuring the effectiveness, compliance, and continuous improvement of our Quality Management Systems (QMS) in alignment with ISO 9001:2015 standards. This role supports and educates business units to ensure quality processes are consistently applied, effectively documented, and continuously improved.

In addition to its strategic and collaborative responsibilities, this position also carries an administrative component, including the management of system workflows, audit documentation, and quality records. The Systems Specialist acts as a key liaison between quality systems and operational teams, driving audit readiness, process integrity, and system excellence across the organization.

Maintain and improve process management systems, including workflow administration and system documentation.
Develop and maintain quality documentation such as work instructions, templates, and process guides to ensure clarity and compliance.
Administer and enhance defect management systems (e.g., NCR, CAR), including oversight by completing concurrence and verification stages.
Collaborate with cross-functional teams to identify opportunities for continuous improvement and support strategic quality initiatives.
Design, deliver, and support training and onboarding programs for internal teams and business users on quality systems and processes.
Conduct process audits (Audit Lites) and process confirmations to ensure compliance with ISO 9001:2015 and internal standards.
Support the development, tracking, and communication of team KPIs and quality performance metrics.
Coordinate and support external audits by managing logistics, communications, and post-audit actions.

Education: Diploma or bachelor’s degree.
2-5 years of relevant experience in quality systems, process improvement, or a similar role.
Familiarity with ISO 9001:2015 is considered an asset.
Exposure to or certification in Lean, Six Sigma, or other continuous improvement methodologies is an advantage.
Change management and/or PMP is an asset.
Ability to analyze and improve business processes using structured problem-solving techniques.
Training or facilitation experience is an asset.
Proficiency in documentation development, workflow administration, and system maintenance.
Strong communication and interpersonal skills to engage with cross-functional teams and stakeholders.
Excellent organizational and time management abilities, with the capacity to manage multiple priorities.
Demonstrated ability to collaborate, influence, and build relationships across departments.
Stakeholder management skills, including the ability to educate and support business users in adopting quality practices.

Due to the nature of work Irving Shipbuilding does, all successful applicants must meet requirements for the Canadian Controlled Goods Program (CGP), Canadian Government Security clearance, and U.S. International Traffic in Arms Regulations (ITAR).

Please note this position requires a full-time, in-office presence.

\n\n Founded in 1882, J.D. Irving, Limited (JDI) has operations in Canada and the United States and are a team of 20,000 dedicated employees. At J.D. Irving, Limited, you are part of a dynamic team of professionals who lead with integrity and are passionate about delivering results. With a culture that nurtures talent and creates an inclusive workplace, you can grow your career across our various operating divisions.\n\n\n We are committed to creating accessible environments for our colleagues, candidates, and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary, or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities.\n\n\n Worried you do not meet all the requirements? Studies have shown that many applicants apply only to job opportunities when they feel they meet 100% of the criteria. We promote an inclusive environment where everyone is appreciated, recognized, and empowered to contribute fully. If you are interested in this position but are worried you did not meet all the requirements, we would encourage you to still apply.\n\n\n We appreciate your interest in our company however only those candidates selected for an interview will be contacted.","hiringOrganization":{"@type":"Organization","name":"J.D. Irving, Limited","sameAs":"https://www.jdirving.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dartmouth, NS, Canada","addressCountry":"Canada","addressRegion":"North America"}}}},{"@type":"ListItem","position":13,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-01","description":"

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

Quality Systems Specialist with experience in the pharmaceutical industry with:

Knowledge in Quality Systems and SOP.
Strong knowledge of relevant GMP, FDA, 21 CFR Part 11 and Data Integrity Regulations (Risk Assessment, Data Mapping, etc), EU regulations and the ability to interpret and apply them for intended use.
Proficient knowledge of computer systems (Microsoft Office etc.) with data collection software (database) and applications like Infinity and SAP.
Solid ability for analyzing data, detecting deviations, inconsistencies and interpret sampling test results.
Proficient knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe).

Qualifications

Bachelor’s degree in science (Chemical, Engineering, Biology, Pharmacy or Microbiology)
Six (6) years of experience in project management, investigations or relevant roles and responsibilities
\nin the pharmaceutical industry.
Fully bilingual (Spanish/English) communication skills, both written and verbal.
Technical and scientific capability to make firm decisions and recommendations.
Microsoft Office, SAP, Infinity

Additional Information

All your information will be kept confidential according to EEO guidelines.

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Quality Systems Lead

As a purpose-led, performance-driven organisation, Blackmores Group strives to create remarkable employee experiences through supporting a diverse and inclusive culture, creating leadership that inspires high performance, and providing everyone with opportunities to achieve their professional, personal and wellbeing goals supported by our flexible work practices and family friendly policies.

Blackmores Group operates in 11 markets, with headquarters in Sydney, an international state-of-the-art manufacturing facility in Braeside, Victoria and additional offices in South East Asia and China.

This is a hybrid role, where 2 days from home and 3 days in an office in Sydney – we have offices in Surry Hills, just beside the Central train station or Warriewood in the northern beaches – with carparking or public transport options available. This role is expected to work based out from our Warriewood campus.

Purpose of role:

The Quality Systems Lead is to support the maintenance and continuous improvement of the Quality Management System (QMS) by providing accurate reporting, data analysis, and system oversight. The role will ensure that quality processes are effectively monitored, documented, and aligned with compliance requirements. Utilization of tools such as Power BI and trend analysis will be key to enabling data-driven decision-making across the organization.

This role reports to a Quality Manager - Systems and Culture and is looking for an independent contributor, builder, multi-tasker and eager to take ownership on continuous improvement to the QMS and deliver continuous improvement on a quality focused culture.

Responsibilities include:

Quality Management Systems: Maintain Quality Management Systems, ensure documentation, procedures and policies align with regulatory and company requirements and implement the better system as needed. Monitor and analyse quality metrics, driving data-based decision-making for improvements.
Culture & Continuous Improvement: Champion a culture of quality by promoting best practices, training and engagement across teams. Develop and deliver training programs to enhance quality awareness and system adherence. Lead initiatives to enhance employee ownership of quality and continuous improvement.
Compliance & Risk Management: Ensure adherence to regulatory requirements, industry standards and customer expectations. Identify and mitigate quality risks through proactive assessment and improvement plans that will be achieved not to rely on electronic system too much, seek a sustainable approach considering business continuity. Collaborate with leadership to align quality objectives with Blackmores strategy.
Leadership & Stakeholder Management: Act as key point of contact for Quality Systems related matters. Partner with operational teams to embed quality-driven processes. Provide leadership in resolving quality-related systems issues and driving root cause analysis. internal and external stakeholders to ensure alignment with medical and regulatory expectations.

Who are you?

At least five years of experience in Quality with proven track record of leading teams to implement and develop or enhance high-quality management systems.
Demonstrated leadership capability with proven experience in driving high quality execution and cross functional work
Possesses logical thinking skills that enable them to identify fundamental principles and persist in problem-solving, even when working with unfamiliar systems.
Experience with Power BI or similar data visualization/reporting tools.
Strong analytical and problem-solving skills with the ability to interpret trends from complex datasets.
Ability to thrive in a fast-paced, highly agile workplace.

Preferred Qualifications and Skills

A Bachelor’s Degree in Science, Pharmacy, Chemical Engineering or any tertiary education related to quality field.
A background in quality with working knowledge of TGA regulations.
Proven relationship-building skills and the ability to establish new links with external stakeholders.
Strong organisational aptitude and the ability to work collaboratively within cross-functional teams.

What we offer:

Great benefits to support your health and wellbeing, including access to free and discounted products and additional leave for your wellbeing
Profit share, we all work together to make profit so we all get a share!
Mental health support for you and your family through our Sonder assistance program
Opportunities to support your local community through paid community leave

Agencies please note: this recruitment assignment is being managed directly by Blackmores Talent Acquisition team. We will reach out to our preferred agency partners if required. Your respect for this process is appreciated.

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Job Description Summary

We are seeking a Quality Systems Leader to oversee and continuously improve our Quality Management System (QMS). This strategic role ensures compliance with regulatory and internal standards while leading key quality processes such as Complaints Management, Quality Management Review, and Annual Product Review. The ideal candidate brings strong leadership, deep knowledge of quality systems, and a passion for driving operational excellence in a dynamic, patient-focused environment.

GE HealthCare Ireland Limited, located in Carrigtohill, Co. Cork, is a global leader in the manufacture and distribution of X-ray and MRI Contrast Media. As part of our Pharmaceutical Diagnostics (PDx) business, we are committed to delivering the right dose to the right patient at the right time. Our modern, agile site supports patients worldwide with high standards of safety, quality, and compliance, contributing to life-changing diagnostic procedures every day.

Job Description

Responsibilities

Lead and maintain core quality systems including CAPA, Change Control, Document Management, Training, Audit Management, and Risk Management.
Oversee the complaints handling process, ensuring timely investigation, root cause analysis, and implementation of effective corrective and preventive actions.
Lead the preparation and execution of periodic QMRs, ensuring comprehensive analysis of quality system performance.
Manage the APR process to ensure timely and accurate review of product quality data and implementation of improvements.
Ensure the QMS meets all relevant regulatory requirements and support audits and inspections.
Identify and implement improvements to quality systems to enhance efficiency and compliance.
Lead and develop a team of quality professionals, fostering a culture of accountability and learning.
Develop and report on key quality metrics and communicate performance to senior leadership.
Oversee the quality training program to ensure employees are trained and competent.
Lead risk assessments and mitigation strategies related to quality systems and compliance.

Qualifications and Requirements

Bachelor’s degree in a scientific, engineering, or related discipline (Master’s preferred) or equivalent.
Strong experience in Quality Assurance or Quality Systems in a regulated industry.
Solid experience in people leadership, including team development and coaching.
Strong knowledge of global regulatory requirements and standards
Proven leadership experience with cross-functional teams.
Excellent communication, analytical, and problem-solving skills.
Experience with electronic QMS platforms (e.g., Veeva, TrackWise, MasterControl)

Desired Skills

Lean Six Sigma or similar continuous improvement certification.
Experience in leading regulatory inspections.
Ability to influence and drive change in a matrixed organization.

Inclusion and Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Behaviors

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

#LI-BG1

#LI-onsite

Additional Information

Relocation Assistance Provided: No

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Company:

The Boeing Company

Position Overview:

Boeing Commercial Airplanes is seeking talented individuals for a Quality Systems Specialist to support our Interiors Responsibility Center in North Charleston, SC.

Position Responsibilities:

Reviews proposals, contracts, regulatory, program and customer requirements ensuring early quality involvement in program development.
Collect, analyze, and interpret supplier quality and supply chain data to identify trends, patterns, and opportunities for improvement
Prepares and maintains Quality directives, policies, processes, procedures and metrics to assure program, contract, customer, regulatory requirements, international standards and working agreements are deployed.
Analyzes process data, metrics, models and flows to identify root cause of problems.
Participates with stakeholders to develop potential preventive or corrective actions and implementation.
Identify key performance indicators (KPIs) and develop metrics to measure the effectiveness of risk.
Conducts research, compiles and analyzes performance reports and process control statistics, to continuously improve process capability.
Conducts quality source selection and process reviews of suppliers' ability to meet program quality requirements and support business decisions, and develops a coordinated response for management review and approval.
Conducts hardware, software and system level audits to determine compliance with quality management system standards, configuration assurance, related business, regulatory and customer requirements and reports results to management.
Analyzes data to provide material review dispositions for nonconforming materials, parts and equipment.
Works under general direction

Basic Qualifications (Required Skill/Experience):

Minimum of 3 years' of experience converting data into meaningful information and communicating the information via data visualizations tools, including Tableau and PowerBI
Minimum of 3 years experience developing and maintaining relationships and partnerships with customers, stakeholders, peers, and partners
Minimum of 1 year experience with SQL
Minimum of 1 year experience communicating and presenting with the ability to effectively convey complex information to various audiences
Minimum of 1 year experience in monitoring risks and compliance requirements

Preferred Qualifications (Desired Skills/Experience):

Experience with R or Python
Experience with Business Intelligence, Data Analytics, or similar role, with a focus on supplier performance analysis
Experience in the aerospace industry
Strong problem-solving skills and the ability to think critically and strategically

Drug Free Workplace:

Boeing is a Drug Free Workplace where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies.

Total Rewards:

At Boeing, we strive to deliver a Total Rewards package that will attract, engage and retain the top talent. Elements of the Total Rewards package include competitive base pay and variable compensation opportunities.

The Boeing Company also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including health insurance, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and a number of programs that provide for both paid and unpaid time away from work.

The specific programs and options available to any given employee may vary depending on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements.

Please note that the information shown below is a general guideline only. Pay is based upon candidate experience and qualifications, as well as market and business considerations.

summary pay range: $100,300 - $135,700

Language Requirements:

Not Applicable

Education:

Not Applicable

Relocation:

Relocation assistance is not a negotiable benefit for this position.

Export Control Requirement:

Safety Sensitive:

This is not a Safety Sensitive Position.

Security Clearance:

This position does not require a Security Clearance.

Visa Sponsorship:

Employer will not sponsor applicants for employment visa status.

Contingent Upon Award Program

This position is not contingent upon program award

Shift:

Shift 1 (United States of America)

Stay safe from recruitment fraud! The only way to apply for a position at Boeing is via our Careers website. Learn how to protect yourself from recruitment fraud - Recruitment Fraud Warning

Boeing is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law.

EEO is the law

Boeing EEO Policy

Request an Accommodation

Applicant Privacy

Boeing Participates in E – Verify

Right to Work Statement

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Our mission

At Vertical Aerospace, we are pioneering the way for electric aviation. The VX4, our eVTOL (electric, vertical, take-off and landing), 'zero emissions' aircraft will set a new safety standard for how we will navigate the sky.

We won't realise our mission following the same legacy processes and traditions our predecessors followed, instead, we want to 'redefine' aerospace best practices.

We are growing quickly from a prototype business to a scaling SME, and the next few years will be critical to our success and delivering on our ambitious goals of having the VX4 in service by 2030.

What to expect

We’re looking for an experienced Quality Systems Engineer to join our fast-growing company. The ideal candidate will have experience of working in Quality Management Systems within a highly regulated environment (ideally Aerospace), or within a start-up environment that is designing and building new advanced electric powered technology.

The candidate will be responsible for ensuring that all products and systems meet the rigorous aerospace industry legal and regulatory standards as we as our customer requirements. You will play a key role in maintaining compliance with the regulatory bodies and driving continual improvement across the businesses processes.

The candidate must be capable of working autonomously within a highly technical environment, able to communicate at all levels and ensure quality initiatives are well embedded in the company culture. The key requirement of this role is to drive the quality culture in Vertical forwards whilst maintaining our core values.

This role will be based out of Vertical's headquarters in Bristol, with regular presence required on-site here and at our test facilities in Kemble.

What you'll do

Develop, implement and maintain the organisations Quality Management Systems. Ensuring all documentation, including Quality manual, procedures and work instructions, are in compliant to ISO90001, AS9100 and other aerospace standards (Part 21 - Production Organisation Approval)
Develop operational system in line with business strategy with support from key stakeholders and subject matter experts.
Prepare and lead ISO9001 and AS9100 internal audits, driving corrective actions.
You will conduct root cause analysis and implement corrective and preventative actions for non-conformances.
You will support and maintain the external audit accreditation activity.
You will interface with regulatory bodies during audits and inspections
Develop, maintain and analyse Quality Metrix and KPI’s to identify trends and areas for continual improvement.
You will play a key role in ensuring that quality processes and quality control is applied to all aspects of the aircraft build.
You will support training initiatives and promote a culture of quality and compliance across the organisation.

What you'll bring

A proven track record of deploying a quality culture in a fast-paced and dynamic Aerospace production work environment.
Demonstrable hands-on experience in Quality Systems and Control and be able to demonstrate a proficient use of Quality and/or Integrated Management Systems.
Excellent stakeholder management, with the ability to work cross-functionally
Excellent communication, documentation and problem-solving skills.
A strong understanding of AS9100, ISOI9001 and aerospace compliance requirements.
Experienced with ISO9001 internal auditing (preferably AS9100-2016).
Experience managing ISO certified management systems
Knowledge of quality tools and Six Sigma methodologies and can demonstrate good problem-solving skills
A degree or the equivalent engineering qualification (HND/HNC).

Desirable Experience:

Experience of regulatory requirements in an aerospace approved organisation
ISO 9001:2015 or higher qualification
Knowledge and experience of regulatory requirements – CAA part 21.
Lean Six sigma qualification (i.e. green belt)
Experience in training or development of others
Knowledge of NADCAP requirements and special process audits

What can you expect from us?

We're on a mission. Where others see limits, we see opportunity, and we work at pace. Working at Vertical isn't your average role but for those seeking a challenge, a flexible, supportive organisation and an incredible team; working here is an opportunity to do the best work of your career.

Our approach promotes ingenuity and courage, while our environment builds success through diligence in safety and being open in the way we work. The only way we're going to assure the next chapter of aviation history is by working as a team, relentlessly, towards our goal.

Our benefits

Our people matter - we're not going anywhere without them. Which is why our company benefits go beyond the essentials.

26 days holiday, plus bank holiday
5 extra days per year to buy (or sell)
5 extra days holiday when you get married or enter a civil partnership
Additional 4% of your salary to spend on extra benefits
Award-winning digital health and wellbeing service (Help@Hand)
Company performance based bonus - rewarding company and individual performance
Company Share Scheme - open to every Vertical employee
Company Pension Scheme - 5% and we match it
Breakfast on us, every day

We may just be the hardest job you've ever had, but we're confident it will be the most rewarding. Join the team today and help us shape the future of Advanced Air Mobility.

Disclaimer Statement

We encourage you to apply even if you may not have all the experience listed in the advert. We recognise that talent comes in various forms and we are committed to providing opportunities that create an environment of growth, diversity, and inclusion for everyone. As part of our desire to review and make our processes fair, we may ask you questions related to these aspects during the application process. For more information on how we will use your data, see our Legal section.

","hiringOrganization":{"@type":"Organization","name":"Vertical Aerospace","sameAs":"https://vertical-aerospace.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bristol Office / Kemble, Cotswolds","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":18,"item":{"@type":"JobPosting","title":"Quality Systems Engineer","datePosted":"2025-08-05","description":"

Company Description

Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We are Making Possible™ products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, advance sustainability, circularity and transparency, and better connect brands and consumers. We design and develop labeling and functional materials, radio frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information that improves the customer experience. Serving industries worldwide — including home and personal care, apparel, general retail, e-commerce, logistics, food and grocery, pharmaceuticals and automotive — we employ approximately 35,000 employees in more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at www.averydennison.com.

Job Description

Avery Dennison is seeking a Graphics Divisional Quality Systems Engineer based at our Fairport Harbor location that is a highly motivated individual contributor with a drive to learn and develop a system that will detect and contain known quality defects. In this role, responsibilities will include managing and implementing the Graphics vision systems and improving processes and measurement systems to align with the expectations of the OEM market. The successful candidate will work independently with minimal direction to navigate the system software, create recipes connecting the system to material, and develop solutions by utilizing systems and process improvement.

Travel Estimated 10%

Activities may include, but are not limited to:

Technical and Operational support of the vision systems currently installed on Graphics production assets
Development of new recipes, classification libraries and processes/ techniques that support our vision systems
Improving inspection capabilities, features, and processes for existing recipes
Collaborating cross-functionally with Engineering, Controls, and IT to support vision system integration with various systems and databases across the site
Educating and driving commitment within the operations team to ensure full utilization of the vision systems.
Creating work instructions as required to enable proper training
Communicating system progress, capabilities and insights to the leadership and support teams, supporting problem solving efforts with inspection data analytics.
Scoping and leading CapEx projects to expand vision system capabilities on additional assets across Graphics
Developing and supporting custom tools and applications, leveraging inspection data to solve problems or simplify processes
Leading external discussions with the OEM to troubleshoot, improve or maintain the vision system
Reading and interpreting OEM manuals to create logic required for defect detection and recipe development
Primary owner of all maintenance and calibration required for vision systems
Aid in the implementation of Automotive Core Tools such as FMEA, SPC, MSA, and Process Capability by evaluating current processes and equipment
Lead ongoing improvement initiatives to meet OEM specified quality standards and customer requirements and developing capabilities to measure with the vision systems
Ability to flex schedule to to support a 24-7 operations schedule as required for escalations or training
Perform other tasks or project work as assigned

Qualifications

Essential:

Bachelor’s Degree in Technical field such as Electrical Engineering, Mechanical Engineering, Chemical Engineering or equivalent from an accredited university
2 years manufacturing experience
Demonstrated trouble-shooting and critical thinking skills
Achieves goals with minimal direction and actively seeks knowledge with a keen attention to detail
Proven capacity to quickly comprehend information from written manuals or complex instruction sets and translate it into effective real-world solutions
Demonstrated decision-making and problem-solving experience
Must be able to actively contribute in a team based environment
Must have schedule flexibility for occasionally staying over or coming in early
Basic understanding of Python functions, libraries, & syntax
Basic understanding of SQL & database structures
Basic understanding of Statistics and various statistical tools
Proficient in Google Suite
Self-directed, self-starter

Preferred:

Proficient with data analysis libraries in Python (i.e. pandas, Numpy, Matplotlib, etc,)
Experience with PostgreSQL
Familiarity with Dr. Schenk’s i4.viz & i4.phc applications
Familiarity with Dr. Schenk’s database structures
Familiarity with Industry 4.0 concepts and middleware
Prior experience with recipe development for vision systems
Prior experience applying statistics to draw conclusions from large datasets
Operations experience within Avery Dennison

Additional Information

The salary range for this position is $68k- $90k/ year.

The base salary range above represents what Avery Dennison reasonably expects to pay for this position as of the date of this posting. Actual salaries will vary within the range, and in some circumstances may be above or below the range, based on various factors including but not limited to a candidate’s relevant skills, experience, education and training, and location, as well as the job scope and complexity, responsibilities, and regular and/or necessary travel required for the position, which may change depending on the candidate pool. Avery Dennison reserves the right to modify this information at any time, subject to applicable law.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status, or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines.

Reasonable Accommodations Notice

If you require accommodations to view or apply for a job, alternative methods are available to submit an application. Please contact (440) 534-6000 or NA.TA.Operations@averydennison.com to discuss reasonable accommodations.

","hiringOrganization":{"@type":"Organization","name":"Avery Dennison","sameAs":"https://www.averydennison.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Painesville, OH, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":19,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-11","description":"Quality Systems Specialist

Company:

Jeppesen Sanderson Inc

Jeppesen A Boeing Company Total Quality is seeking a Quality Systems Specialist to support our Digital Aviation Solutions business. Join a growing team focused on ensuring quality & compliance across a diverse portfolio of solutions including flight navigation, safety operations, crew efficiency, and airplane health. This position is perfect for someone excited by the world of aviation and eager to work in a collaborative environment to deliver innovative products to airline customers. Business travel may be required as needed.

You will join a global team of quality professionals and serve as an independent quality consultant providing end-to-end quality management support to all leadership levels, business units, and functional organizations. Primary assignments involve activities that require knowledge of the quality discipline and aviation regulatory requirements.

While the work is based in Colorado, Washington, or Texas, part of the team is located across Europe, which does necessitate some early morning meetings. Most team members are currently working a hybrid model spending 2-3 days per week in the office with a flexible schedule.

Position Responsibilities:

Serves as subject matter expert to management and special external spokesperson to the Federal Aviation Administration (FAA) for the organization on major matters pertaining to its policies, plans, and objectives
Regularly contributes to the development of new job practices, techniques, and standards. Recognized as a job expert within the Quality organization
Develops solutions to complex problems that require ingenuity and innovation while ensuring alignment with organization objectives
Creates and provides education/coaching on quality services (e.g., audits, problem investigations, continuous improvement, corrective action, and preventive action) and quality management principles
Develops metrics in partnership with business stakeholders which provide quantitative measures regarding process health to enable data-based decision making
Performs audits (i.e., product, system, and process) to determine conformance with industry standards (e.g., ISO 9001, DO-200, AS9100) as well as regulatory and customer requirements
Works with higher level management to implement process improvements impacting multiple organizations and locations
Performs work with minimal direction and exercises considerable latitude in determining objectives and approaches to assignments
Continuously seeks to expand and improve personal knowledge in quality management best practices

Basic Qualifications (Required Skills/Experience):

5+ years of experience with Quality Management Systems (QMS)
5+ years of experience utilizing process improvement and problem-solving methodologies
3+ years of experience working with regulatory agencies (FAA, EASA and/or CASA)
Visual, oral, and written communication skills
15% travel

Preferred Qualifications (Desired Skills/Experience):

Experience with FAA Letters of Acceptance (LoA)
ISO-9001:2015 lead auditor certification
Experience working with RTCA DO-200B/ED-76A and AC 20-153B
ASQ, CQA or other professional certifications
Six Sigma Green Belt highly desired
Experience working in SAFe or Agile teams

Drug Free Workplace:

Pay & Benefits:

Pay is based upon candidate experience and qualifications, as well as market and business considerations.

Summary Pay Range: $107,100.00-$144,900.00

Language Requirements:

Not Applicable

Education:

Not Applicable

Relocation:

Relocation assistance is not a negotiable benefit for this position.

Export Control Requirement:

This is not an Export Control position.

Safety Sensitive:

This is not a Safety Sensitive Position.

Security Clearance:

This position does not require a Security Clearance.

Visa Sponsorship:

Employer will not sponsor applicants for employment visa status.

Contingent Upon Award Program

This position is not contingent upon program award

Shift:

Shift 1 (United States of America)

Stay safe from recruitment fraud! The only way to apply for a position at Boeing is via our Careers website. Learn how to protect yourself from recruitment fraud - Recruitment Fraud Warning

EEO is the law

Boeing EEO Policy

Request an Accommodation

Applicant Privacy

Boeing Participates in E – Verify

Right to Work Statement

","hiringOrganization":{"@type":"Organization","name":"Boeing","sameAs":"https://www.boeing.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"USA - Englewood, CO, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":20,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-08","description":"

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

Quality Systems Specialist with experience in the pharmaceutical industry with:

Knowledge in Quality Systems and SOP.
Strong knowledge of relevant GMP, FDA, 21 CFR Part 11 and Data Integrity Regulations (Risk Assessment, Data Mapping, etc), EU regulations and the ability to interpret and apply them for intended use.
Proficient knowledge of computer systems (Microsoft Office etc.) with data collection software (database) and applications like Infinity and SAP.
Solid ability for analyzing data, detecting deviations, inconsistencies and interpret sampling test results.
Proficient knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe).

Qualifications

Bachelor’s degree in science (Chemical, Engineering, Biology, Pharmacy or Microbiology)
Six (6) years of experience in project management, investigations or relevant roles and responsibilities
\nin the pharmaceutical industry.
Fully bilingual (Spanish/English) communication skills, both written and verbal.
Technical and scientific capability to make firm decisions and recommendations.
Microsoft Office, SAP, Infinity

Additional Information

All your information will be kept confidential according to EEO guidelines.

","hiringOrganization":{"@type":"Organization","name":"QRC Group","sameAs":"https://www.qrcgroup.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Manatí, Manatí, Puerto Rico","addressCountry":"Puerto Rico","addressRegion":"North America"}}}},{"@type":"ListItem","position":21,"item":{"@type":"JobPosting","title":"Quality Systems Engineer","datePosted":"2025-08-12","description":"

Care to Find Solutions

Join a team of good people doing good work with intent. People like you, who care to make a difference.

About the opportunity

In this exciting role as a Senior Quality Engineer – Manufacturing for Respiratory and Acute Care (RAC), you'll actively collaborate with Operations, Production, and Process Development teams. Your QMS and statistical expertise will be key in providing training and guidance to uphold quality standards for both new and existing processes. Additionally, you will contribute to identifying and implementing improvements in our Quality Management System. A practical attitude, coupled with a willingness to collaborate, is crucial for success in this role, alongside a proactive nature and results-focused approach.

Offering involvement across every function of the business and exposure to a variety of products and manufacturing processes, this full-time position at our Auckland site will help you develop a strong understanding of the broader business. This sets the stage for an exciting array of career advancement options within F&P.

About you

5+ years of work experience in Quality Engineering in the medical device industry.
A tertiary qualification in Science or Engineering.
Working knowledge of standards and regulations (ISO13485, ISO14971, 21 CFR Part 820, MDR).
Experience with process and test method validation activities.
Working knowledge of statistics and process improvement tools.
Six Sigma or CQE certification is preferable

You will also have:

Excellent communication skills both written and verbal with the ability to share complex ideas, positively influence, negotiate, and challenge with tact and diplomacy.
Strong problem-solving ability, (both through your own independent thinking and collaboration across the business) and a strong resilience when navigating problems.
An ability to build relationships at all levels within the organization.

Working With Us

Employee share purchase scheme
Bi-annual Profit share
Generous Paid Parental Leave
Life, Critical illness and Income Protection Insurance
Discounted Health Insurance
Active Social clubs & community groups
In-house training programs from external providers
Purchasing privileges for Fisher & Paykel Healthcare and Medela products
School holiday programme subsidy
Banking and Insurance discounts
Free Parking
Beautiful campus with green spaces
Subsidised Café’s
Annual Salary Review
High rates of internal promotion

Access to state-of-the-art facilities

About Us

Fisher & Paykel Healthcare is a world leader in the design, manufacture, and marketing of medical devices, exporting to over 120 countries globally.

Our commitment to care unites us. Here, we’re driven to improve patient care and outcomes through inspired and world-leading healthcare solutions.

Care to join us? Apply today

We focus on nurturing a positive and inclusive culture based on trust and respect. In New Zealand, our employee-led communities, Spectra (rainbow), Manaaki (Māori) and Women in Engineering play an important role in this culture. We also have a commitment to creating a positive lasting impact on society, shown by our support of New Zealand organisations such as Diversity Works NZ, Pride Pledge and Global Women.

This is a full-time, permanent position (40 hour week) with a salary range of $85,000 NZD to $110,000 NZD. The role is based in our Auckland office in Highbrook Drive in East Tamaki

","hiringOrganization":{"@type":"Organization","name":"Fisher & Paykel Healthcare","sameAs":"https://www.fphcare.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"East Tamaki, NZ, 2013","addressCountry":"New Zealand","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":22,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-11","description":"

Howmet Aerospace, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries. The Company’s primary businesses focus on jet engine components, aerospace fastening systems and titanium structural parts necessary for mission-critical performance and efficiency in aerospace and defense applications, as well as forged wheels for commercial transportation. Howmet Aerospace is transforming the next phase of more fuel-efficient, quieter aerospace engines and sustainable ground transportation. For more information, visit www.howmet.com. Follow @howmet: Twitter, Instagram, Facebook, LinkedIn and YouTube.

Job Summary

This Quality Systems Specialist position will support the administration of quality manuals, continuous improvement initiatives & interaction with business center personnel on quality initiatives. Application of root cause analysis & corrective/preventative action as appropriate. This position will be responsible to:

Support Quality Management System for assigned plant

Manage internal audit program and conduct annual internal audits per AS9100/AS13100 requirements.
Coordinate and support external audits for certification bodies E.g. AS9100, Nadcap.
Coordinate and support customer audits (internal & external)
Review and implement quality system changes.
Corrective Action Board (CAB) meeting administrator
Participate in Corporate Quality meetings

Support supplier partnerships

Drive root cause on CARs to reduce incoming material issues
Coordinate and support supplier on-site visits for audits and problem solving
Provide feedback to BU Supplier Quality on Supplier scorecards for OTD and PPM

QE Support

Customer communication for certification/problem resolution.

Job Responsibilities

Systems thinker--sees the business and its operation holistically; understands actions and reactions; considers multiple pathways of potential effect before decisions; thinks strategically about interventions with an eye toward scale
Optimizer--constantly challenging the organization to work smarter; supports others to ensure they have what they need to do their work successfully
Anticipation--looks ahead to minimize potential issues and maximize advantages; prepares others for what comes next
Operational accelerator--drives continuous improvement; understands ramifications of automation and other advances; advocates for safety, ergonomics and scalable solutions
Organization and structure--works within existing structures while striving to improve and standardize them; provides accurate information; galvanizes others toward common goals
Influence--leverages knowledge, relationship, data and perspective to persuade, educate and navigate; gains buy in and adoption of ideas and practices at scale; interacts with a variety of stakeholders
Data informed--focused on things that drive quantifiable business outcomes; evaluates based on quantitative feedback; knows and explains the “why” behind actions
Prioritized reaction--handles the unexpected without losing sight of important objectives; reacts where greatest leverage points exist
Relationship--connects individually and with teams across shifts and practices; builds rapport and commonality; creates a “win together” ethic; serves as liaison between shop floor and engineering; keeps the pulse of the floor; helps people feel heard

Basic Qualifications:

Associates Degree with 5 years quality experience in a manufacturing environment with quality management systems responsibilities OR 10 years of progressive experience in quality in a manufacturing environment, investment casting and quality management systems responsibilities
Employees must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available for this position.
This position entails access to export-controlled items and employment offers are conditioned upon an applicant's ability to lawfully obtain access to such items.

Preferred Qualifications

BS Degree in Business or Engineering from an accredited institution.
Quality System audit experience is preferred.
Excellent communication, negotiation, and interpersonal skills.
Self-starter and ability to manage multiple projects.
Demonstrates competent use of automated order system.
Solid base knowledge of manufacturing process and flow of material.
Strong quantitative analysis skills, including the use of Microsoft Excel.
Ability to develop and use planning strategies.

\nHowmet 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.\n\nEqual Opportunity Employer:\n\n\n\n\n Howmet is proud to be an Equal Employment Opportunity employer. We are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other applicable legally protected characteristics.\n \n\n\n\n If you need assistance to complete your application due to a disability, please email TalentAcquisitionCoE_Howmet@howmet.com","hiringOrganization":{"@type":"Organization","name":"Howmet Aerospace","sameAs":"https://www.howmet.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hampton, VA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":23,"item":{"@type":"JobPosting","title":"Quality Systems Engineer","datePosted":"2025-08-14","description":"

Join our innovative team

Want to do more than just imagine the ways our world will move tomorrow? Here’s your opportunity. Join the technology company that’s transforming the future of mobility today.

About this position

In this role, the successful candidate will play a key part in maintaining and supporting the organization’s Quality Management System (QMS) along with other related business systems.

Your role

Global:

Support the global Quality organization with Quality Management System development and other Quality standard operating systems
Ensure compliance to our Quality procedures and maintenance of our Quality Certifications
Upgrade Global standards for QMS management, and develop Quality OS for all Quality functions (Supplier, SW Quality, Design Quality, Plant and Customer)
Orchestrate Internal and External Quality Audits - IATF 16949, VDA6.3, VDA FFA, Customer Specific, Aptiv EOS, QS2.0, etc.
Maintain system to monitortrained global auditors.
Maintain system to ensure compliance to Customer Specific Requirements and standards.
Work with the Auditors and Natural Owners to close any Non-conformances
Organize the required Annual Management Reviews

Regional/Local:

Coordinate the creation of new processes and procedures to facilitate the implementation of Quality Systems (EOS / STAGES).
Support the recruitment of employees and professional training of the department employees in Quality System activities.
Support the creation of new Quality training programs and online training software (Aptiv Academy). Coordinate the activities of System, Process and Product Audits.
Control and organize the information of changes in EOS (DCR), customer specific requirements and official technical standards, making their disclosure as necessary and applicable to each sector of the site. Be the DCC (Document Control Center) coordinator.
Manage, coordinate and implement the Quality Management System (EOS/STAGES) in accordance withnational, international and customer specific standards.
Report to the management the status of the quality system (results of System, Process and Customer Audits) and compliance with the respective corrective actions.
Supporting and collaborating with other locations cross region within the Quality System Organization
Maintain core of certified Auditors onsite to conduct Internal Audits
Work with the Auditors and Natural Owners to close any Non-conformances at the site/region.
Organize the required site Annual Management Reviews

Your background

MSc/BSc degree in Engineering, preferred in quality
2 years of relevant experience
Standard knowledge: ISO 9001; IATF 16949; preferred: VDA 6.3; VDA 6.5
Knowledge of various quality system methodologies and automotive core tools: 8D problem solving, 5-Why, Ishikawa Diagram, PFMEA, CP, SPC, Kaizen, 5S, APQP, PPAP, Continuous Improvement
Fluent English language knowledge – spoken and written
MS Office user level is essential

Why join us?

You can grow at Aptiv. Aptiv provides an inclusive work environment where all individuals can grow and develop, regardless of gender, ethnicity or beliefs.
You can have an impact. Safety is a core Aptiv value; we want a safer world for us and our children, one with: Zero fatalities, Zero injuries, Zero accidents.
You have support. We ensure you have the resources and support you need to take care of your family and your physical and mental health with a competitive health insurance package.

\"Only applications with resumes in English will be reviewed.\"

#LI-KK2

Privacy Notice - Active Candidates: https://www.aptiv.com/privacy-notice-active-candidates

Aptiv is an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender identity, sexual orientation, disability status, protected veteran status or any other characteristic protected by law.

","hiringOrganization":{"@type":"Organization","name":"Aptiv","sameAs":"https://www.aptiv.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"PRT Braga Mfg., Portugal","addressCountry":"Portugal","addressRegion":"Europe"}}}},{"@type":"ListItem","position":24,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-14","description":"Quality Systems Specialist

Company:

The Boeing Company

Boeing Commercial Airplanes (BCA) is seeking an Experienced Quality Systems Specialist (Level 3) to join our Fabrication Quality team onsite in Auburn, Washington.

As a Quality System Specialist, you will act as the primary focal to interface with Boeing Business Partners and the Federal Aviation Administration on various complex Quality Management System related topics and issues.

Candidates may be required to travel to other Boeing sites per business needs.

Position Responsibilities:

Leads Quality reviews of proposals, contracts, regulatory, program and customer requirements ensuring early quality involvement in program development
Develops Quality budget and cost estimates. Leads multi-function, multi-site groups to develop company directives, policies, processes, procedures and metrics to assure program, contract, customer, regulatory requirements, international standards and working agreements are deployed
Leads stakeholders in analysis of process data, metrics, models and flows to identify root cause of complex problems and development and implementation of preventive or corrective actions
Conducts research, compiles and analyzes performance reports and process control statistics to continuously improve process capability
Conducts quality source selection and process capability assessments of suppliers' ability to meet program quality requirements and support business decisions
Develops Quality criteria for supplier source selection and a coordinated response for review and approval by senior management
Develops scope, schedule, plans and leads hardware, software and system level audits to determine compliance with quality management system standards, configuration assurance, related business, regulatory and customer requirements, and reports results to management
Trains senior management on preparation for third party audits
Analyzes data to provide material review dispositions for complex nonconforming materials, parts and equipment
Assists in the development of new standard repairs for nonconforming materials, parts and equipment
Works under minimal direction

Basic Qualifications (Required Skills/Experience):

3+ years of experience in developing and writing processes, policies, and procedures
3+ years of experience with Quality Management Systems (QMS) and/or Boeing Production System (BPS)
3+ years of experience in applying verbal and written communication skills including spelling, grammar, punctuation, form and style, proof reading and editing skills
3+ years of hands-on experience using Microsoft Office Products like Word, Outlook, PowerPoint, and Excel
Able to occasionally travel domestically, work flexible hours, overtime and occasional weekends when necessary

Preferred Qualifications (Desired Skills/Experience):

3+ years of experience working in Aerospace, Manufacturing, Quality, or experience in a regulated industry
Customer focused ability to work independently or as part of a team

Drug Free Workplace:

Boeing is a Drug Free Workplace where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria are met as outlined in our policies.

Union:

This is a Non-union represented position.

Total Rewards

Pay is based upon candidate experience and qualifications, as well as market and business considerations.

Summary pay range: $86,700- $117,300

Language Requirements:

Not Applicable

Education:

Not Applicable

Relocation:

Relocation assistance is not a negotiable benefit for this position.

Export Control Requirement:

This position must meet export control compliance requirements. To meet export control compliance requirements, a “U.S. Person” as defined by 22 C.F.R. §120.15 is required. “U.S. Person” includes U.S. Citizen, lawful permanent resident, refugee, or asylee.

Safety Sensitive:

This is not a Safety Sensitive Position.

Security Clearance:

This position does not require a Security Clearance.

Visa Sponsorship:

Employer will not sponsor applicants for employment visa status.

Contingent Upon Award Program

This position is not contingent upon program award

Shift:

Shift 1 (United States of America)

Stay safe from recruitment fraud! The only way to apply for a position at Boeing is via our Careers website. Learn how to protect yourself from recruitment fraud - Recruitment Fraud Warning

EEO is the law

Boeing EEO Policy

Request an Accommodation

Applicant Privacy

Boeing Participates in E – Verify

Right to Work Statement

","hiringOrganization":{"@type":"Organization","name":"Boeing","sameAs":"https://www.boeing.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"USA - Auburn, WA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":25,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-18","description":"We anticipate the application window for this opening will close on - 29 Aug 2025

A Day in the Life

Medtronic is a world leader in providing health care products that restore health and extend life.  The Medtronic Diabetes R&D team contributes directly to this mission; we deliver software and firmware for Medtronic’s pump and continuous glucose monitoring devices. 

Our business is growing significantly as the market demands reliable medical devices which look and feel more like consumer devices.  We are looking for an Associate Quality Systems Specialist who can help us continue to make devices more robust and reliable for our patients.

This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.

Engineers create our market-leading portfolio of innovations. Join us to make a lasting impact. Help bring the next generation of life-changing medical technology to patients worldwide. This is a unique opportunity to apply your best technical innovation, problem solving and leadership skills to improving how people live their lives every day. 

Minimum Requirements:

Requires a Baccalaureate degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.

NICE TO HAVE:

Intermediate or better level of experience with Microsoft suite, including but not limited to Word, Excel, SharePoint, Teams, PowerPoint and Adobe
Experience with Oracle Agile, Trackwise and/or PowerBI systems
Experience in FDA, Certifying Body and/or Notified Body audits/inspections
Experience or training in project management
Experience with medical device industry Regulations, Standards and Quality Management Systems

Other Responsibilities:

Supports the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
Conduct quality reviews of Change Orders for Quality Management System documents and records.
Provides expertise and guidance to stakeholders in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
Supports audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
Prepares reports and/or necessary documentation, data analysis, etc. and provides to applicable stakeholders.
Co-ordinates implementation of enterprise changes within local quality management system.
Co-ordinates legal requests in support of government investigations or litigations.
Ensures the quality assurance programs and policies are maintained and modified regularly.
Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.
Leads smaller quality projects and project teams, while facilitating larger quality projects in a variety of roles

SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages tasks or project actions assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals

DIFFERENTIATING FACTORS

Autonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments

Innovation and Complexity:

Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex .
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area

Communication and Influence:

Communicates primarily and frequently with internal contacts.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making. Superior internal customer service is a must

Leadership and Talent Management:

May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream

U.S. Pay Transparency (for SIP, Commission, Hourly Direct, Interns, Executives)

Physical Job Requirements

Benefits & Compensation

Salary ranges for U.S (excl. PR) locations (USD):$72,800.00 - $109,200.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Further details are available at the link below:

Medtronic benefits and compensation plans

About Medtronic

Learn more about our business, mission, and our commitment to diversity here.

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Great on-site culture and attractive pay rates
Perfect central regional location in Australia – close to Melbourne and Sydney!
Outstanding rotating roster for work life balance

Are you looking for a tree change? Discover Tumut, a scenic town in the Snowy Mountains region of New South Wales, where adventure and relaxation meet. Whether you enjoy hiking, fishing, snowboarding, or simply exploring beautiful landscapes, it’s easy for this welcoming town to feel like home.

Our world class pulp and paper mill in Tumut produces high-quality kraft paper for domestic and international markets. As one of the world’s most sustainable kraft paper mills, you’ll work with best-in-class technology, surrounded by a friendly community and an easy commute to work. For the right candidate, we offer relocation and visa sponsorship support (based on eligibility criteria). Make the Snowy Mountains your new home and join us in creating a better world, together.

Role details

This is a key role which offers tremendous growth through involvement. The successful incumbent possesses excellent communication and analytical skills, detail-orientated, and always aiming for the best performance.

Ideally you have experience with working on and developing final product quality management systems in a fast-paced Manufacturing, heavy industrial, FMCG, or highly processed environment where continuous improvement and lean manufacturing are a normal part of your everyday.

This position works closely with internal paper mill and Visy group-based operations, technical and logistics teams (both paper and board), to ensure our final paper product qualities meet customer requirements and that the process and quality systems ensure customer complaints and claims are resolved and prevented.

Daily interaction with the sales team is essential and interaction with customers directly is required from time to time. Confidence and professionalism will see you succeed in this highly interactive environment while strong administrative, data processing & analysis skills and background knowledge in paper and/or board manufacturing and quality will give you the edge to perform well.

This is a full time Monday to Friday (standard 37.5 working hours) with an on-call every 5 weeks for the technical team after-hours support for the Laboratory, Analytical online instruments, and Quality monitoring.

What you’ll do

Monitoring & reporting on paper quality, quality non-conformances, quality audits & capability.
Recommend & implement quality processing changes to prevent non-conformances.
Review laboratory test results & liaise with laboratory team regarding any observations or requirements.
Manage paper mill quality management system specifications & system improvements; investigate system issues.
Management of paper complaints & claims, investigations and corrective actions with the support of the operations, technical and sales teams.
Liaise with sales and customers and do potential customer site visits, inspections and recommendations to improve linerboard performance as required.
Provide Customers as well as Sales with technical support, on request, which includes product compliance data, answering questionnaires and product sample requests.
Manage and coordinate, together with stakeholders, the paper hold stocks & quarantine stocks decision making and volumes.

Your success will come from

Your ability to work collaboratively, with internal stakeholders within the Operations Team to improve quality processes in the production environment, creating a culture of Continuous Improvement with regard to Quality, and improve the use of lead indicators for critical decision making.
The strong relationships you establish with external stakeholders (customers and suppliers) to manage expectations and responses to quality incidents, collecting and analyzing critical data to enhance decision making and feedback to improve internal systems.

What you will bring

Ideally you will have a Tertiary Qualification in Applied Science or equivalent
Experience working in a Quality Co-Ordinator/Assurance role in paper or board making including paper testing or packaging or food and beverage industry (advantageous)
Strong MS Excel or Data Analysis software capabilities
Highly organised, task focused with strong administrative and technical report writing skills
Knowledge and understanding AS4801 and ISO9001 standards, maintaining NCR database, CAR investigations and worked with QMS systems
You will be analytical, and data driven, with a pro-active approach to identifying, investigating and root cause analysis solving problems.
Able to work in a hot environment with stairs and confined spaces
Team player with a focus on safety and continuous improvement
Excellent work ethic and self driven to succeed to get the job done.

What you’ll love when you join us

Sustainability: Contribute to sustainability initiatives that make a difference.
Supportive Environment: Be part of a team that values safety, respect, and collaboration.
Career Growth: Opportunities for further training and career advancement within the company

Ready to make a difference? Apply now and be a key player in shaping our future!

You will be required to meet Visy’s employment criteria which will include a criminal history check and pre-employment medical (including drug & alcohol testing)
Visy is an equal opportunity employer committed to providing a working environment that embraces and values diversity and inclusion.
These roles are only open to candidates currently residing in Australia with full working rights.

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At Saputo, we bring good to the table by making high-quality products, investing in our people, and supporting communities around the world . As a top 10 global dairy processor, we value contributions that matter and strive to foster an inclusive, growth-driven work environment. Ready to bring your best?

We’re looking for a detail-oriented and tech-savvy Quality Systems Administrator to support our quality systems and data processes. If you enjoy working with SAP, Excel, and quality data, this could be the role for you!

Play a key role in our Quality Systems Team - based at our Southbank head office or one of our manufacturing sites.

How you will make contributions that matter

As a Quality System Administrator, you will be responsible for setting up, managing, and supporting quality information systems including SAP QM master data, SharePoint pages and other platforms. You’ll work closely with internal teams and external partners to ensure data integrity, compliance, and continuous improvement.

Set up and manage SAP QM / PM data and inspection plans.
Maintain testing schedules, calibration plans, and certificates.
Support SAP MDG workflows and inspection types across systems.
Monitor SAP QM interfaces and resolve lab/instrument issues.
Create contaminant certificates and BI templates.
Provide training and support for quality systems.
Contribute to investigations and projects work.

About you

Diploma in Food Science, Laboratory Technology, or related field (preferred).
Experience in Food Science, QA, or Laboratory roles.
Advanced Microsoft Excel skills and SAP QM experience.
Knowledge of laboratory operations and dairy testing methodologies (preferred).
Excellent communication, problem-solving, and relationship management skills.

We’ll support you with

The opportunity to make contributions that matter, whilst being supported by multinational, values led company
A competitive annual salary
Learning and development opportunities with the ability to grow in your own way
Ability to participate in our Employee Share Ownership Program
Product Discounts and other employee benefits

Click \"Apply\" to submit your application. For a confidential discussion, please contact Manisha at 0498 147 768.

Saputo Dairy Australia is an equal opportunity employer. Applications close on 1st September, but we may progress sooner, so apply as soon as possible. All applicants require Australian working rights at the time of applying. We are a 2025 Circle Back Initiative Employer and commit to respond to every applicant.

As a leading dairy processor in Australia, Saputo produces, markets, and distributes a variety of products, with a portfolio of well-loved brands such as Devondale, Liddells, CHEER, Mersey Valley and Tasmanian Heritage. Our people bring these popular brands to life, while servicing our farming communities and through our AG Warehouse network.

Whether your expertise lies in manufacturing, operations, supply chain, sales, quality assurance, or in any other function, your role is integral to our success. You will make contributions that matter, all while working alongside colleagues who genuinely care about your success and who will roll up their sleeves to help.

","hiringOrganization":{"@type":"Organization","name":"Saputo Inc.","sameAs":"https://www.saputo.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Burnie, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":28,"item":{"@type":"JobPosting","title":"Quality Systems Leader","datePosted":"2025-08-13","description":"

Overview

The Quality Systems Leader is responsible for ensuring the implementation, maintenance, and continuous improvement of an effective Quality Management System (QMS) at the site. This role drives cross-functional alignment to uphold compliance, foster a strong quality culture, and ensure all materials and processes meet defined standards. Additionally, the position supports the development of operational excellence by mentoring and coaching Polymer Specialists and Operations Star Points in quality system awareness and best practices.

Responsibilities

Quality Management System (QMS) Leadership

Ensure the development, implementation, maintenance, and continuous improvement of the site’s Quality Management System (QMS).
Maintain compliance with ISO 9001 and IATF 16949:2016 standards, ensuring the integrity of the QMS during planned changes.
Promote the process approach, risk-based thinking, and the importance of an effective QMS across the organization.
Maintain and update the Quality Manual and Quality Procedures.
Organize and lead Management Review Meetings to report on QMS performance and identify improvement opportunities.

Customer and Regulatory Compliance

Represent the voice of the customer in internal processes, ensuring customer requirements are understood and met.
Review customer specifications versus site capabilities and communicate gaps to management.
Coordinate and lead customer audits, visits, and responses to customer questionnaires and quality notifications.
Ensure externally provided processes, products, and services do not compromise product conformity or customer satisfaction.
Communicate the importance of meeting customer, statutory, and regulatory requirements across the organization.

Audit and Performance Monitoring

Lead internal and external audits of the QMS and ensure timely closure of corrective action plans.
Lead the Internal Quality Audit team and plan annual audits.
Report weekly metrics for Quality Notifications and Block Stock.
Monitor and analyze quality performance indicators to identify strategic improvement opportunities.

Management of change (TA’s) & Product or Raw material qualifications

Ensure changes to process technology, equipment, suppliers, outside services, adhere to all requirements of the QMS.
Provide input to changes related to product and raw material qualifications.
Ensure proper management of changes documentation is defined, created, and retained.

Training, Coaching, and Communication

Develop and deliver training on quality systems and standards to internal teams.
Mentor and coach Polymer Specialists and Operations Star Points to build quality awareness and capability.
Communicate quality-related issues, events, and system updates to site leadership and stakeholders.
Represent the site in regional and corporate quality network meetings and collaborate with sister site quality leaders.

Qualifications

High School Diploma or equivalent required. Associate’s or Bachelor’s degree preferred
3–5 years of experience in a quality role within a manufacturing environment required
1–2 years of experience in a leadership capacity strongly preferred

Certifications (preferred but not required)

Certified Quality Auditor
ISO 9001 / IATF 16949 Lead Auditor certification

Technical Knowledge

Strong understanding of ISO 9001, IATF 16949
Experience with quality tools such as FMEA, SPC, CAPA, root cause analysis, and risk management
Familiarity with statistical analysis and quality metrics

Skills & Competencies

Excellent analytical, problem-solving, and decision-making skills
Strong communication and interpersonal skills across all levels of the organization
Ability to lead cross-functional teams and drive continuous improvement
Skilled in planning, organizing, and managing multiple priorities
Capable of mentoring and coaching others in quality principles and practices

","hiringOrganization":{"@type":"Organization","name":"Celanese","sameAs":"https://celanese.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Richmond, VA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":29,"item":{"@type":"JobPosting","title":"Quality Systems Coordinator","datePosted":"2025-08-20","description":"

Your Impact
As Quality Systems Coordinator at our Huntingwood, NSW site, you’ll take ownership of integrated quality and food safety systems, ensuring compliance with regulatory and third-party standards. You’ll also drive continuous improvement to enhance product quality, operational effectiveness, and overall site performance.

Key Responsibilities

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Manage and maintain Quality & Food Safety Systems (FSSC, HACCP, GMP)
\n
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Lead site audits, document control, and effective CAPA implementation
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Conduct internal audits, gap analyses, and coach teams on compliance
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Champion continuous improvement initiatives to lift quality outcomes
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Facilitate workshops to strengthen quality culture across operations
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Support central Quality projects and standardised system improvements
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About You

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Proven experience in Quality, Production or CI roles within FMCG manufacturing
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Strong knowledge of GFSI standards (FSSC, SQF, BRC), HACCP, GMP & SOPs
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Continuous improvement mindset with Lean, Six Sigma or TQM experience
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Collaborative communicator with strong problem-solving skills
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Tertiary qualification in Food Science/Technology or related discipline valued
\n

Why Asahi Beverages?
At Asahi Beverages, we're passionate about crafting more than just drinks – we craft moments of connection, celebration, and shared enjoyment. We bring together a diverse portfolio of iconic beverage brands, a commitment to quality, and a drive to constantly innovate. Headquartered in Melbourne and with facilities right across Australia and New Zealand, you’ll find Asahi is a place where talent is nurtured, and ambition is rewarded. If you’re ready to toast your future, we’re ready to meet you.

We are a Circle Back Initiative employer and commit to responding to all applicants.

","hiringOrganization":{"@type":"Organization","name":"Asahi Beverages","sameAs":"https://www.asahi.com.au/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"NSW - other","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":30,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-19","description":"

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Summary of Role

The role is to implement and execute tasks relating to day-to-day Quality Assurance aspects. The role entails taking responsibility for Quality Assurance matters around processes and documentation in the City North business unit.

Key Responsibilities

Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department.
Writing and reviewing SOP's, Work Instructions, BPR's and Forms.
Writing and reviewing of Deviations, Non-Conformance reports, Corrective Action Requests and prepare the final report for QP review.
Follow up on change control actions with appropriate action owners and drive for on time closure of actions.
Prepare Quarterly reports for each site.
Prepare Product Quality Review reports.
Prepare & present Monthly/Annual Metrics.
Complete complaints investigations and assist with close out of complaints.
Perform cGMP internal audits.
Assist in the performance of external audits (as required).
Responsible for executing training for quality & other relevant persons.
Assist with preparation for customer/regulatory audits.
Assist with audit requests during customer/regulatory audits.
Prepare responses to customer audits.
Host/attend cross departmental meetings as required as quality representation.
Identify and support opportunities for improving processes and or procedures.
To undertake such tasks and to manage specific or ad hoc projects as and when required to meet department and business needs and within the scope of the job-holder’s capabilities.
Carry out various other additional tasks that may be required from time to time in accordance with the overall goal of the company

Knowledge / Skills & Experience

Essential:

Bachelor’s or associate degree or Diploma / Certificate in GMP, Regulatory and Compliance or similar. May substitute experience in lieu of educational requirements.
1+ years’ experience working in GMP or Regulated Environment
Ability to manage multiple tasks and set priorities.
Problem Solving and Troubleshooting skills. The successful candidate should display a dynamic and proactive approach to manage problems.
Self-motivated with a results driven approach.
Adaptable and ability to work collaboratively.
Proficient in Microsoft Office products (incl. Excel, PowerPoint, Word, etc.)
Driving Licence Required.

Desirable:

Experience in Lean Manufacturing, including experience in Lean tools to develop continuous improvements.

#LI-MS1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

","hiringOrganization":{"@type":"Organization","name":"PCI Pharma Services","sameAs":"https://pci.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"IRL City North, Ireland","addressCountry":"Ireland","addressRegion":"Europe"}}}},{"@type":"ListItem","position":31,"item":{"@type":"JobPosting","title":"Manager, Quality Systems","datePosted":"2025-08-15","description":"

Anduril Industries is a defense technology company with a mission to transform U.S. and allied military capabilities with advanced technology. By bringing the expertise, technology, and business model of the 21st century’s most innovative companies to the defense industry, Anduril is changing how military systems are designed, built and sold. Anduril’s family of systems is powered by Lattice OS, an AI-powered operating system that turns thousands of data streams into a realtime, 3D command and control center. As the world enters an era of strategic competition, Anduril is committed to bringing cutting-edge autonomy, AI, computer vision, sensor fusion, and networking technology to the military in months, not years.

ABOUT THE JOB:

The Business Systems team is responsible for building and improving the many business systems that enables Anduril to accomplish its mission. Anduril’s supply chain, accounting, sales & growth, engineering, field maintenance, quality, manufacturing, and many more teams rely on the technology built by us. We work across the company to ensure we have the tools and capabilities necessary for mission success.

As Manager of Quality Systems, you will be the leader of Anduril’s “Quality Operating System (QualOS for short)”, which is a cross-discipline team of PMs, Engineers (software and analytic), solution and business process architects, and other technologist responsible for delivering solutions that enable the performance of Anduril’s Quality organizations. To accomplish this, you will partner with multiple stakeholder teams including Quality Engineering, Reliability, Configuration Management, Production/Manufacturing, Supply Chain, Test & Evaluation, Analytics, and more to identify and deploy technology solutions that accelerate their work. You will develop a detailed understanding of each team’s challenges and requirements to understand what solutions can best address their needs. You will architect and build solutions, drive adoption, and enable best practices for scale and efficiency. Because these teams have different use cases and timelines, you must be an agile, general-athlete style PM who can pivot from deep diving the intricacies of how one team executes a technical workflow, to closely examining the metrics of the systems to understand where the failure points are, to mapping an intertwined set of dependencies to build a roadmap, to updating executives on the current and future sets of your program all in the course of a single day.

WHAT YOU\"LL DO:

Developing the QualOS vision for Anduril, ensuring that our internal tech stack maximizes the impact of Quality users across the hardware development cycle, making one of our Quality engineers as effective as five at traditional manufacturers.
Serve as the “single threaded leader” for QualOS, orchestrating the investment made by many teams (Software PM and engineers, Analytics Engineers, Solution and Business Architects, Sysadmins, etc.) within the Corporate Technology department and be the point of contact between CorpTech and all Quality departments at the company.
Setting the QualOS roadmap, ensuring it maximizes business impact and solves the most pressing problems in order of importance
Communicating across stakeholders on your program's development and roadmap, as well as monitoring and reporting on program performance to understand if business outcomes are getting met
Driving adoption and enablement through the use of change management tools, schedules, and user engagement (UAT, training, sandbox environment, piloting, etc).

REQUIRED QUALIFICATIONS:

7+ years in Product or Program Management, dealing with both technical and non-technical teams
Strong understanding of Manufacturing and Quality processes
Excellent written / verbal communication and project management skills
Ability to think systemically, take decisive action quickly, and above everything else, find a way for the business to win
Deeply analytical in nature, with the ability to harness data to drive decisions and build solutions to capture and enrich data where it is lacking
Experience with coordinating and directing the effort made by a wide variety of technologist skillsets, including software development (PMs and engineers), enterprise systems (solution architects, solution engineers, sys admins), and data (analytic and data engineers, data analysts)
Experience with quality management processes, including: Non-Conformance Management, Corrective And Preventative Actions, Supplier Quality, and Risk Mitigation
Strong working knowledge of AS9100 and ISO9001
Expertise in the development of both 1P (built) and 3P (bought) enterprise systems, with strong understanding of: access controls / security, infrastructure, feature development, configuration, administration, integrations, etc.
Strong critical thinking skills, with the ability to challenge traditional approaches when it comes to developing technology solutions rather than just default to “buy new shiny software” mentality
Demonstrated success decomposing a problem into addressable component parts and arranging the correct sequencing
Proven ability to “see around corners” by crafting a strategy for 12-18 months into the future
Must be able to travel up to 33% of the time, as your stakeholders will be geographically dispersed
Must be eligible to obtain and maintain a U.S. security clearance

US Salary Range$182,000—$273,000 USD

The salary range for this role is an estimate based on a wide range of compensation factors, inclusive of base salary only. Actual salary offer may vary based on (but not limited to) work experience, education and/or training, critical skills, and/or business considerations. Highly competitive equity grants are included in the majority of full time offers; and are considered part of Anduril's total compensation package. Additionally, Anduril offers top-tier benefits for full-time employees, including:

Platinum Healthcare Benefits: For U.S. roles, we offer comprehensive medical, dental, and vision plans at little to no cost to you.\n
- For UK roles, Private Medical Insurance (PMI): Anduril will cover the full cost of the insurance premium for an employee and dependents.
- For AUS roles, Private health plan through Bupa: Coverage is fully subsidized by Anduril.
\n
Basic Life/AD&D and long-term disability insurance 100% covered by Anduril, plus the option to purchase additional life insurance for you and your dependents.
Extremely generous company holiday calendar including a holiday hiatus in December, and highly competitive PTO plans.
16 weeks of paid Caregiver & Wellness Leave to care for a family member, bond with your baby, or tend to your own medical condition.
Family Planning & Parenting Support: Fertility (eg, IVF, preservation), adoption, and gestational carrier coverage with additional benefits and resources to provide support from planning to parenting.
Mental Health Resources: We provide free mental health resources 24/7 including therapy, life coaching, and more. Additional work-life services, such as free legal and financial support, available to you as well.
A professional development stipend is available to all Andurilians.
Daily Meals and Provisions: For many of our offices this means breakfast, lunch and fully stocked micro-kitchens.
Company-funded commuter benefits available based on your region.
Relocation assistance (depending on role eligibility).
401(k) retirement savings plan - both a traditional and Roth 401(k). (US roles only)

The recruiter assigned to this role can share more information about the specific compensation and benefit details associated with this role during the hiring process.

Anduril is an equal-opportunity employer committed to creating a diverse and inclusive workplace. The Anduril team is made up of incredibly talented and unique individuals, who together are disrupting industry norms by creating new paths towards the future of defense technology. All qualified applicants will be treated with respect and receive equal consideration for employment without regard to race, color, creed, religion, sex, gender identity, sexual orientation, national origin, disability, uniform service, Veteran status, age, or any other protected characteristic per federal, state, or local law, including those with a criminal history, in a manner consistent with the requirements of applicable state and local laws, including the CA Fair Chance Initiative for Hiring Ordinance. We actively encourage members of recognized minorities, women, Veterans, and those with disabilities to apply, and we work to create a welcoming and supportive environment for all applicants throughout the interview process. If you are someone passionate about working on problems that have a real-world impact, we'd love to hear from you!

To view Anduril's candidate data privacy policy, please visit https://anduril.com/applicant-privacy-notice/.

","hiringOrganization":{"@type":"Organization","name":"Anduril","sameAs":"https://www.anduril.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Costa Mesa, California, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":32,"item":{"@type":"JobPosting","title":"Manager, Quality Systems","datePosted":"2025-08-15","description":"

ABOUT THE JOB:

WHAT YOU\"LL DO:

Developing the QualOS vision for Anduril, ensuring that our internal tech stack maximizes the impact of Quality users across the hardware development cycle, making one of our Quality engineers as effective as five at traditional manufacturers.
Serve as the “single threaded leader” for QualOS, orchestrating the investment made by many teams (Software PM and engineers, Analytics Engineers, Solution and Business Architects, Sysadmins, etc.) within the Corporate Technology department and be the point of contact between CorpTech and all Quality departments at the company.
Setting the QualOS roadmap, ensuring it maximizes business impact and solves the most pressing problems in order of importance
Communicating across stakeholders on your program's development and roadmap, as well as monitoring and reporting on program performance to understand if business outcomes are getting met
Driving adoption and enablement through the use of change management tools, schedules, and user engagement (UAT, training, sandbox environment, piloting, etc).

REQUIRED QUALIFICATIONS:

7+ years in Product or Program Management, dealing with both technical and non-technical teams
Strong understanding of Manufacturing and Quality processes
Excellent written / verbal communication and project management skills
Ability to think systemically, take decisive action quickly, and above everything else, find a way for the business to win
Deeply analytical in nature, with the ability to harness data to drive decisions and build solutions to capture and enrich data where it is lacking
Experience with coordinating and directing the effort made by a wide variety of technologist skillsets, including software development (PMs and engineers), enterprise systems (solution architects, solution engineers, sys admins), and data (analytic and data engineers, data analysts)
Experience with quality management processes, including: Non-Conformance Management, Corrective And Preventative Actions, Supplier Quality, and Risk Mitigation
Strong working knowledge of AS9100 and ISO9001
Expertise in the development of both 1P (built) and 3P (bought) enterprise systems, with strong understanding of: access controls / security, infrastructure, feature development, configuration, administration, integrations, etc.
Strong critical thinking skills, with the ability to challenge traditional approaches when it comes to developing technology solutions rather than just default to “buy new shiny software” mentality
Demonstrated success decomposing a problem into addressable component parts and arranging the correct sequencing
Proven ability to “see around corners” by crafting a strategy for 12-18 months into the future
Must be able to travel up to 33% of the time, as your stakeholders will be geographically dispersed
Must be eligible to obtain and maintain a U.S. security clearance

US Salary Range$182,000—$273,000 USD

Platinum Healthcare Benefits: For U.S. roles, we offer comprehensive medical, dental, and vision plans at little to no cost to you.\n
- For UK roles, Private Medical Insurance (PMI): Anduril will cover the full cost of the insurance premium for an employee and dependents.
- For AUS roles, Private health plan through Bupa: Coverage is fully subsidized by Anduril.
\n
Basic Life/AD&D and long-term disability insurance 100% covered by Anduril, plus the option to purchase additional life insurance for you and your dependents.
Extremely generous company holiday calendar including a holiday hiatus in December, and highly competitive PTO plans.
16 weeks of paid Caregiver & Wellness Leave to care for a family member, bond with your baby, or tend to your own medical condition.
Family Planning & Parenting Support: Fertility (eg, IVF, preservation), adoption, and gestational carrier coverage with additional benefits and resources to provide support from planning to parenting.
Mental Health Resources: We provide free mental health resources 24/7 including therapy, life coaching, and more. Additional work-life services, such as free legal and financial support, available to you as well.
A professional development stipend is available to all Andurilians.
Daily Meals and Provisions: For many of our offices this means breakfast, lunch and fully stocked micro-kitchens.
Company-funded commuter benefits available based on your region.
Relocation assistance (depending on role eligibility).
401(k) retirement savings plan - both a traditional and Roth 401(k). (US roles only)

The recruiter assigned to this role can share more information about the specific compensation and benefit details associated with this role during the hiring process.

To view Anduril's candidate data privacy policy, please visit https://anduril.com/applicant-privacy-notice/.

","hiringOrganization":{"@type":"Organization","name":"Anduril","sameAs":"https://www.anduril.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Seattle, Washington, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":33,"item":{"@type":"JobPosting","title":"Quality Systems Admin","datePosted":"2025-08-15","description":"

fairlife, LLC is a Chicago-based nutrition company that creates great-tasting, nutrition-rich and dairy products to nourish consumers.

With over $3B in annual retail sales, fairlife’s portfolio of delicious, lactose-free, real dairy products includes: fairlife® ultra-filtered milk; Core Power® High Protein Shakes, a sports nutrition drink to support post-workout recovery; fairlife® nutrition plan™, a nutrition shake to support the journey to better health.

A wholly owned subsidiary of The Coca-Cola company, fairlife, LLC has been recognized by both Fast Company and Nielsen for its industry leading innovation.

To learn more about fairlife and its complete line of products, please visit fairlife.com.

The construction of fairlife's manufacturing facility in Webster, NY is underway. This state-of-the-art, 750k sq ft, greenfield plant is expected to be operational in late 2025 and will lay the foundation for fairlife's next phase of growth as the leading dairy nutrition provider. While coupling the industry’s latest technologies and fairlife's operational excellence to build this world-class facility, fairlife plans to hire 250 new employees and bring in approximately 5 million lbs. of milk a day, with room to grow over the coming years.

job purpose:

The Quality Compliance Admin provides key support for the Quality Assurance Department and is responsible for the generating and reviewing of daily manufacturing reports to ensure document completion and accuracy of data. Additionally assists the Quality Systems Manager in the daily work requirements, including regulatory compliance, document and records review, and audit program upkeep.

responsibilities:

Primary responsibility is to ensure accuracy and completion of regulatory records. Review of documentation could include but not limited to production worksheets, batch reports, processing charts, and associated processing and packaging logs with immediate escalation and follow up on any identified gaps or non-conformities.
Support internal and external site audit program including any regulatory inspections as needed. Conduct internal inspections with a cross-functional audit team.
Review for accuracy and completion of all CIP records, checklists, and titration records. Monitor sanitation programs for effectiveness through document review and perform any needed tracking associated with these records. Effectively communicate any nonconformances found to site leadership.
Responsible for maintaining all results and reports in a confidential manner in accordance with the Company Letter of Confidentiality. Responsible for managing the record retention program for all required process documentation.
Identify and address any potential food safety/compliance/regulatory issues. This could be the result of documentation issues, laboratory testing results out of specification, processing parameters not achieved, personal observations, employee feedback, etc.
Communicate with production operators to ensure regulatory records are completed properly, as needed.
Provide input and support for quality documents, processes and procedures. Ensure all procedures, work aids, forms, etc. are current and document controlled.
Assist with new hire orientation and provide necessary training for plant personnel on quality management systems as needed.
Assist with quality investigations as needed.
Follow all safety, work policies, and Good Manufacturing Practices (GMP) rules.

skills/qualifications required:

A college degree is preferred or equivalent experience in a manufacturing facility.
Certification in Better Process Control School, HACCP and PCQI (will provide training if needed).
Strong analytical and problem-solving skills with a strong focus on details and accuracy of any required paperwork.
Ability to work independently with professional demeanor.
Effectively able to communicate both verbal and written with various cross-functional teams.
Intermediate computer skills (Word, Excel, Outlook, WMS)
Self-starter and self-motivated with the ability to complete work assignments based on broad directions with minimum supervision.
Knowledge of materials management techniques

working conditions and physical requirements:

40-45 hours/sitting/standing/walking/lifting.
Ability to lift up to 50 lbs. Assist can be provided.

food safety responsibilities:

Notify supervision of any repairs or adjustments that are required that may affect product quality or food safety.
Understand, observe, and comply with the handling and usage of the color-coded container policy while in the Production Areas.
Perform all duties necessary to meet Company, Customer and/or Government requirements/standards as prioritized by the Company.
Ability to initiate action to prevent the occurrence of nonconformities relating to Food Safety and the Quality of the product, processes, quality system, or safety system.
Identify and record any problems relating to Food Safety and the Quality of the ingredients, processes, quality system, or safety system.
Control further processing or delivery of nonconforming product in terms of Food Safety and Quality issues until the deficiency or unsatisfactory condition has been corrected.
In the event of absence, another employee with the same skill level will assume the duties and responsibilities as required.

position location: Webster, NY

reports to: Quality Systems Manager

travel requirements: <10%

exempt/nonexempt: Nonexempt

*Base pay offered may vary depending on geography, job-related knowledge, skills, and experience. A full range of medical, financial, and/or other benefits, dependent on the position, is offered.

Base pay range:$30—$32 USD

fairlife, LLC is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. All qualified applicants and employees will be given equal opportunity. Selection decisions are based on job-related factors.

In addition to its nondiscrimination commitment, the Company will also provide reasonable accommodation of qualified individuals with known disabilities unless doing so would impose an undue hardship on the Company. If you have a disability and would like to request accommodation in order to apply for a position with us, please email careers@fairlife.com.

For Recruitment Agencies

At fairlife, we manage the majority of our hiring internally through our dedicated Talent Acquisition team, which is actively engaged in direct candidate sourcing. Most of our roles are filled through applications submitted via our careers site or through direct outreach by our team.

\n\n

As our recruitment is primarily handled in-house, we work only occasionally with external agencies, and only those on our existing, pre-approved vendor list. At this time, we are not reviewing or expanding that list.

\n\n\n

Unsolicited resumes or submissions from external agencies not authorized by our Talent Acquisition team will be considered direct candidate applications. As such, fairlife will not assume responsibility for any placement fees associated with these submissions.

\n\n
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Overview

Responsibilities

Quality Management System (QMS) Leadership

Ensure the development, implementation, maintenance, and continuous improvement of the site’s Quality Management System (QMS).
Maintain compliance with ISO 9001 and IATF 16949:2016 standards, ensuring the integrity of the QMS during planned changes.
Promote the process approach, risk-based thinking, and the importance of an effective QMS across the organization.
Maintain and update the Quality Manual and Quality Procedures.
Organize and lead Management Review Meetings to report on QMS performance and identify improvement opportunities.

Customer and Regulatory Compliance

Represent the voice of the customer in internal processes, ensuring customer requirements are understood and met.
Review customer specifications versus site capabilities and communicate gaps to management.
Coordinate and lead customer audits, visits, and responses to customer questionnaires and quality notifications.
Ensure externally provided processes, products, and services do not compromise product conformity or customer satisfaction.
Communicate the importance of meeting customer, statutory, and regulatory requirements across the organization.

Audit and Performance Monitoring

Lead internal and external audits of the QMS and ensure timely closure of corrective action plans.
Lead the Internal Quality Audit team and plan annual audits.
Report weekly metrics for Quality Notifications and Block Stock.
Monitor and analyze quality performance indicators to identify strategic improvement opportunities.

Management of change (TA’s) & Product or Raw material qualifications

Ensure changes to process technology, equipment, suppliers, outside services, adhere to all requirements of the QMS.
Provide input to changes related to product and raw material qualifications.
Ensure proper management of changes documentation is defined, created, and retained.

Training, Coaching, and Communication

Develop and deliver training on quality systems and standards to internal teams.
Mentor and coach Polymer Specialists and Operations Star Points to build quality awareness and capability.
Communicate quality-related issues, events, and system updates to site leadership and stakeholders.
Represent the site in regional and corporate quality network meetings and collaborate with sister site quality leaders.

Qualifications

High School Diploma or equivalent required. Associate’s or Bachelor’s degree preferred
3–5 years of experience in a quality role within a manufacturing environment required
1–2 years of experience in a leadership capacity strongly preferred

Certifications (preferred but not required)

Certified Quality Auditor
ISO 9001 / IATF 16949 Lead Auditor certification

Technical Knowledge

Strong understanding of ISO 9001, IATF 16949
Experience with quality tools such as FMEA, SPC, CAPA, root cause analysis, and risk management
Familiarity with statistical analysis and quality metrics

Skills & Competencies

Excellent analytical, problem-solving, and decision-making skills
Strong communication and interpersonal skills across all levels of the organization
Ability to lead cross-functional teams and drive continuous improvement
Skilled in planning, organizing, and managing multiple priorities
Capable of mentoring and coaching others in quality principles and practices

","hiringOrganization":{"@type":"Organization","name":"Celanese","sameAs":"https://celanese.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Richmond, VA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":35,"item":{"@type":"JobPosting","title":"Quality Systems Coordinator","datePosted":"2025-08-25","description":"

Our Company

Biocare Medical, LLC is an innovator in developing and supplying world class automated immunohistochemistry instrumentation, and the full range of reagents for IHC lab testing. Biocare specializes in high quality IHC, ISH, and FISH slide staining through its brand-new automated instrument, NeoPATH Pro™, and offers best-in-class simultaneous Multiplex IHC solutions.

The company’s customers include clinical histology laboratories, pharmaceutical companies, CROs, biotechnology companies as well as academic, government, military, and non-profit laboratories. Biocare Medical offers an expanding portfolio of integrated products to address the rapidly growing cancer and infectious disease diagnostic and research markets with novel tissue immunohistochemistry and in situ hybridization methods. Biocare Medical is headquartered and has manufacturing facilities in California with a global distribution network.

Summary/Objective

The Quality Systems Coordinator is responsible for maintaining and supporting the company’s Quality Management System (QMS), with a primary focus on document control and quality system records. This role ensures that quality documents—such as standard operating procedures, forms, and policies—are created, reviewed, approved, and maintained in accordance with internal procedures and applicable regulatory requirements (e.g., ISO 13485, MDSAP, FDA QSR, and EU IVDR). The coordinator also provides administrative support for QMS processes including change control, internal audits, and training records, and supports compliance activities such as CAPAs, nonconformances, and complaint handling. The ideal candidate will be detail-oriented, organized, and able to work collaboratively with cross-functional teams to uphold quality standards and regulatory compliance. This is an individual contributor role with no leadership responsibilities

Essential Functions

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Maintain the Document Control System and support the overall Quality Management System (QMS) in accordance with applicable regulatory requirements (e.g., ISO 13485, MDSAP-participating countries, FDA Quality System Regulation, and EU IVDR), including the routing, approval, archival, and periodic review of controlled documents such as SOPs, forms, and policies.
Coordinate and track document change requests in accordance with internal procedures and regulatory requirements (e.g., ISO 13485, MDSAP-participating countries, FDA Quality System Regulation, and EU IVDR).
Support the administration and maintenance of document control systems, including PolicyTech, Tableau, Monday or similar platforms.
Manage and monitor QA-Tickets, ensuring timely response and proper documentation of requests (e.g., document changes, process clarifications, quality queries).
Ensure timely periodic review and update of controlled documents; issue reminders and track compliance across departments.
Act as subject matter expert (SME) for document control processes and provide guidance and training to internal stakeholders.
Assist in tracking and ensuring QMS conformance to maintain certification status with MDSAP and other relevant audits or inspections.
Support quality system compliance activities such as CAPAs, nonconformances (NCs), and complaint investigations, under the direction of the Quality Compliance team.
Prepare document control and QMS performance metrics; contribute to Management Reviews by providing data trends and summaries.
Assist during internal and external audits (e.g., MDSAP, ISO, FDA) by organizing, retrieving, and verifying documentation and ensuring traceability.
Collaborate cross-functionally to identify and implement improvements in documentation workflows and quality recordkeeping practices.
Support onboarding and ongoing training of personnel in document control procedures and QMS-related software systems.
Perform other duties as assigned to support Quality Assurance and regulatory compliance.
Other duties as assigned by Management.

Competencies

Associate’s or Bachelor’s degree in a life science, quality, or related field is required, or equivalent work experience in a regulated industry.
Working knowledge of QMS requirements for medical devices and IVDs, including document control, training, change control, and audit support.
Strong accuracy and organizational skills for managing controlled documents and QMS records in a regulated environment.
Able to understand and interpret quality procedures, regulatory requirements, and technical documentation.
Skilled in writing and formatting SOPs, forms, and other controlled documents in a clear, compliant, and user-friendly manner.
Applies sound decision-making within defined policies; able to prioritize and manage tasks independently with minimal supervision.
Experienced with quality systems software (e.g., PolicyTech, Tableau, MasterControl, Monday) and Microsoft Office tools.
Familiar with FDA QSR, ISO 13485, MDSAP, ISO 14971, and EU IVDR as they apply to QMS maintenance and document control.
Works effectively across departments to ensure documentation compliance and support quality system activities.

Compensation Range

$28 - $33 Hourly

Expected Hours of Work

8:00 a.m. to 5:00 p.m. Monday – Friday. This position may require extended weekday or weekend hours depending on business needs.

Full-Time Positions Offer

Company Sponsored Health Insurance - Medical, Dental, Vision
Company Sponsored Life Insurance
Voluntary Benefits
Retirement plan with a match - 401(k)
PTO
Paid Holidays
EAP

BioCare Medical values the diversity of individuals, ideas, and perspectives, and what they bring to the workplace. We know that our people represent the future of the company, so we only hire the best from around the world. Applications from all qualified candidates will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, physical or mental disability, or status as a Protected Veteran.

All inquiries strictly confidential.

","hiringOrganization":{"@type":"Organization","name":"Biocare Medical, LLC","sameAs":"https://biocare.net/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pacheco, California, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":36,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-22","description":"Quality Systems Specialist

Company:

The Boeing Company

Boeing Commercial Airplanes (BCA) is seeking an Experienced or Senior Quality Systems Specialist (Level 3 or 4) to support the Quality team in Everett, Washington.

We are looking for forward thinking, self-driven Quality professionals to drive changes in a highly collaborative & flexible environment to challenge our current processes by working with Internal stakeholders and suppliers gathering best practices and lessons learned to create standard work tools to drive continuous improvement, expedite effective growth, and facilitate cultural change and improve Suppliers Quality performance.

Position Responsibilities:

Assists in review of proposals, contracts, regulatory, program and customer requirements to prepare quality assurance plans and tests for hardware and software products, processes and services
Maintains Quality directives, policies, processes, procedures and metrics to assure program, contract, customer, regulatory requirements, international standards and working agreements are deployed using established procedures
Collects and verifies data to support the identification of root cause routine problems
Provides ideas and concepts for corrective action development
Supports quality source selection and process reviews of suppliers' ability to meet program quality requirements
Assists with hardware, software and system level audits to determine compliance with quality management system standards, configuration assurance, related business, regulatory and customer requirements
Documents audit results in standard formats
Compiles data and provides recommendations for material review disposition
Works under general supervision

Basic Qualifications (Required Skills/ Experience):

3+ years of knowledge or experience working with and supporting Quality Management Systems or Quality Requirements within a Quality and/or Engineering discipline
3+ years of experience working with quality and/or manufacturing data systems
3+ years in creation, preparation and communication of leadership decks and executive summaries
3+ years of experience with project management
Proficiency and experience with Microsoft Office (Excel, Word, PowerPoint, Visio, MS Project)

Preferred Qualifications (Desired Skills/Experience):

5 or more years’ related work experience or an equivalent combination of education and experience
1+ years of experience with SQL
Experience with Data Analytics, Integrated Quality Data System (IQDS)
Proficiency and experience with CMES, Velocity, Teradata
Technical experience in an aerospace environment

Typical Education/Experience:

Experienced (Level 3):
Education/experience typically acquired through advanced education (e.g. Bachelor) and typically 6 or more years' related work experience or an equivalent combination of education and experience (e.g. Master+4 years' related work experience, 10 years' related work experience, etc.).

Senior (level 4):
Education/experience typically acquired through advanced education (e.g. Bachelor) and typically 10 or more years' related work experience or an equivalent combination of education and experience (e.g. Master+8 years' related work experience, 14 years' related work experience, etc.).

Drug Free Workplace:

Boeing is a Drug Free Workplace (DFW) where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies.

Total Rewards:

Pay is based upon candidate experience and qualifications, as well as market and business considerations.

Summary Pay Range for Experienced (Level 3): $87,000 - $117,000

Summary Pay Range for Senior (Level 4): $107,300 - $145,400

Language Requirements:

Not Applicable

Education:

Not Applicable

Relocation:

Relocation assistance is not a negotiable benefit for this position.

Export Control Requirement:

This is not an Export Control position.

Safety Sensitive:

This is not a Safety Sensitive Position.

Security Clearance:

This position does not require a Security Clearance.

Visa Sponsorship:

Employer will not sponsor applicants for employment visa status.

Contingent Upon Award Program

This position is not contingent upon program award

Shift:

Shift 1 (United States of America)

Stay safe from recruitment fraud! The only way to apply for a position at Boeing is via our Careers website. Learn how to protect yourself from recruitment fraud - Recruitment Fraud Warning

EEO is the law

Boeing EEO Policy

Request an Accommodation

Applicant Privacy

Boeing Participates in E – Verify

Right to Work Statement

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Work. Sunwater is hiring! We’re looking for an experienced Quality and Systems Manager to play a pivotal role in advancing Sunwater’s strategic objectives. This role is responsible for seamlessly integrating our Business (Quality) Management System with other key frameworks - including health and safety, environment, asset management, and information security - to drive continuous improvement, ensure compliance, and enhance operational efficiency and effectiveness.

As part of this role, you’ll lead the development, implementation, and ongoing refinement of a unified Integrated Management System that supports Sunwater’s core operations, projects, and business processes. Your work will ensure alignment with legislative requirements while enabling smarter, more agile ways of working.

This is more than a traditional quality assurance role – it’s about fostering cross-functional collaboration and making our systems work harder and smarter for the entire organisation.

Other key accountabilities include:

Conduct maturity assessments and management systems assurance and lead the development of a risk-based assurance plan to evaluate control effectiveness and drive continuous improvement.
Oversee business performance reporting, including nonconformities, root cause analysis, and corrective actions.
Manage incident investigations and ensure effective implementation of corrective measures to prevent recurrence.
Develop, review, and maintain system procedures and documentation, while providing specialist quality support across Operations, Projects, and Enabling functions.

You’ll bring over 10 years of experience in a comparable role, backed by a degree in Business, Quality, or a related discipline - or equivalent practical expertise. A lead auditor certification in ISO 9001, ISO 14001, and/or ISO 45001 is essential, reflecting your deep understanding of integrated management systems and compliance standards. In addition, you will have:

Effective Communication Skills – Ability to bridge gaps between technical teams and stakeholders, clearly articulating quality standards, risks, and expectations across all levels.
Strategic Leadership – Lead cross-functional teams, align quality goals with business objectives, and foster a culture of accountability and continuous improvement.
Analytics and Problem-Solving Skills – Prioritise assurance activities based on risk to optimise resource allocation and strengthen organisational performance.

This role offers an array of attractive benefits including an attractive base salary, 12.75% superannuation, access to banked time and TOIL, 17.5% leave loading and a genuine emphasis on work/life balance.

Water. Imagine a career where your work truly matters, where you are part of a team that values you and your contributions. At Sunwater, you will bring life’s most essential resource to over 5,000 agriculture, urban and industrial customers, helping to sustain communities and drive water for prosperity across regional Queensland. We share the values of these communities — starting with caring about our people. Engage in fascinating work that is constantly evolving, allowing you to grow and shape a successful career and develop unique skills and experience in an industry brimming with opportunity.

Life. At Sunwater, we believe our employees are our greatest asset, and we are committed to providing the support, resources and benefits that you need to thrive. That's why we offer a range of attractive benefits designed to help you bring your best every day, including:

My benefits: Access employee benefits and discounts hosted by Reward Gateway
My wellbeing: Prioritise your wellbeing with our comprehensive health and wellness offerings and programs
My time: Enjoy flexible working arrangements and the ability to purchase up to 4 additional weeks of leave, ensuring you can tailor your work to fit your lifestyle
My growth: We prioritise your professional growth with career development programs, study assistance, support for professional memberships, and structured early career pathways to help you build a rewarding and successful career

Now is the perfect time to join Sunwater and take advantage of the boundless opportunities for your career today and in the future. We are a diverse team and proud of the unique journeys and stories each of us brings. As we continue to grow, we need more diverse backgrounds and perspectives than ever before. We are committed to a barrier-free recruitment process and work environment. If you require any accommodations, please let us know so we can ensure you can fully participate in our recruitment experience, which includes reference verification, psychometric testing, background checks and a pre-employment medical evaluation to ensure the best fit for our team.

Sunwater acknowledges Aboriginal and Torres Strait Islander peoples as the first peoples of this country and Traditional Custodians of the land and water we rely on. We respect and value their continued sacred connection to Country, including the diverse, rich traditions, languages and customs that are the longest living in the world. We acknowledge their resilience in the face of significant and ongoing historical, cultural, and political change within Australia. We recognise and value the importance of truth-telling today, and our role to listen and learn.

Apply for this role by hitting the Apply button now or visit our website to learn more.

","hiringOrganization":{"@type":"Organization","name":"Sunwater","sameAs":"https://www.sunwater.com.au/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Brisbane","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":38,"item":{"@type":"JobPosting","title":"Quality Systems Engineer","datePosted":"2025-08-26","description":"

At Relativity Space, we’re building rockets to serve today’s needs and tomorrow’s breakthroughs. Our Terran R vehicle will deliver customer payloads to orbit, meeting the growing demand for launch capacity. But that’s just the start. Achieving commercial success with Terran R will unlock new opportunities to advance science, exploration, and innovation, pioneering progress that reaches beyond the known.

Joining Relativity means becoming part of something where autonomy, ownership, and impact exist at every level. Here, you're not just executing tasks; you're solving problems that haven’t been solved before, helping develop a rocket, a factory, and a business from the ground up. Whether you’re in propulsion, manufacturing, software, avionics, or a corporate function, you’ll collaborate across teams, shape decisions, and see your work come to life in record time. Relativity is a place where creativity and technical rigor go hand in hand, and your voice will help define the stories we’re writing together. Now is a unique moment in time where it’s early enough to leave your mark on the product, the process, and the culture, but far enough along that Terran R is tangible and picking up momentum. The most meaningful work of your career is waiting. Join us.

\nAbout the Team\n \nThe Quality team is focused on embedding quality into every part of the design and production process for Terran R. Not just inspecting at the end but influencing how things are built from the start. The team embeds themselves directly within design, manufacturing, test, and launch teams to stay close to the hardware, understand constraints, and proactively shape decisions. As we move beyond initial development into production and then scaled operations, now is the time to put the right processes, controls, and inspections in place without slowing down progress. The team plays a key role in balancing risk, driving a culture of ownership, and ensuring that speed doesn’t come at the cost of reliability. Success here means building a quality system that scales with the Terran R program and Relativity as a whole.\n \nAbout the Role\n \n\nThe Quality Systems Engineer in QMS team will be responsible for developing, implementing, maintaining, and continuously improving our Quality Management System in compliance with AS9100 and applicable aerospace regulations. You will:\n \n• Partner with engineering, manufacturing, supply chain, and leadership teams to ensure our processes are robust, our documentation is clear, and our execution drives mission success. \n• Develop, implement, and maintain the quality management system (QMS) in alignment with AS9100, customer requirements, and regulatory expectations. \n• Lead QMS documentation control system that ensures effective document release, revision control, and accessibility, to support the scale of \n• Manage the internal audits, external audits, and certification activities; track and close out audit findings. \n• Support risk management activities and continuous improvement initiatives. \n• Provide QMS training and guidance to employees at all levels.\n\n \nAbout You - Minimum Qualifications\n \n• Bachelor’s degree in engineering, quality, or related STEM field, or equivalent experience. \n• 3+ years of experience in quality systems or quality engineering, familiar with QMS platforms and digital applications, preferably in aerospace \n• In-depth working experience of AS9100 or ISO9001 requirements and principles. \n• Certified QMS lead auditor (AS9100 preferred). \n• Strong skills in document control, process mapping, and continuous improvement.

At Relativity Space, we are committed to transparency and fairness in our compensation practices. Actual compensation will be determined based on experience, qualifications, and other job-related factors.

Compensation is only one part of our total rewards package. Relativity Space offers competitive salary and equity, a generous PTO and sick leave policy, parental leave, an annual learning and development stipend, and more! To see some of the benefits & perks we offer, please visit here.

Hiring Range:$85,000—$109,000 USD

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

","hiringOrganization":{"@type":"Organization","name":"Relativity","sameAs":"https://www.relativityspace.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Long Beach, California","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":39,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-27","description":"Quality Systems Specialist

Company:

Boeing Defence United Kingdom Limited

Introduction:

Boeing Defence UK (BDUK) Ltd is looking to appoint an Experienced Quality Assurance Specialist to be responsible for the provision of Quality Assurance and Compliance monitoring of the Apache AH-64E LTTSS Programme as part of the wider Vertical Lift platform. The role will be based at Wattisham Flying Station, UK. Travel to other work sites may be required.

About the role:

This is a key role in providing Quality Assurance against regulatory standards and accreditations for the maintenance activities undertaken on the AH-64E aircraft based at Wattisham Flying Station. BDUK’s Quality Management System (QMS) is approved by the Military Aviation Authority (MAA) and meets the requirements of MAOS, DAOS and CFAOS. The BDUK Quality Management System (QMS) is certified to AS9110C / AS9100D with additional accreditations including; ISO 9001, ISO 27001 and ISO 44001.

The company plans to extend the scope of approvals and accreditations to support the expansion of new platforms, programmes and growth opportunities within the UK Defence Environment.

The Quality Assurance Specialist will be responsible for providing assurance of the current regulatory approvals and certifications and supporting the organisation with maintaining compliance with the associated regulatory requirements and standards. The Quality Specialist will be a valued member of the Vertical Lift Quality Team, reporting to the Apache Quality Lead under the direction of the Vertical Lift Quality Manager.

Position Responsibilities:

Provide assurance of the BDUK QMS and its related processes through active engagement with other functions supporting aircraft maintenance activities
Participation in internal audits in support of the BDUK Single Audit Schedule covering both MRP Part 145 regulations and AS9110 / AS9100 Standards
Supporting the BDUK Vertical Lift QA Manager / Lead in the preparation for external quality audits and formulation of any resulting action plans.
Performance of documentation reviews of related quality processes / procedures
Supporting colleagues within other functions with development of processes / procedures to ensure regulatory compliance and adherence to Boeing Pols/Pros
Corrective Action Plan Management (CAPA) including
Co-ordination & facilitation of Root Cause Corrective Action (RCCA)
Establishment & management of local Corrective Action Boards
Verification & Validation of CAPA Implementation
Supporting Safety / Quality investigations (as directed by Lead / Manager)
Non-Conformance Management and inputting data into Boeing software tools.
Leading FOD initiatives and regular walk rounds of Hangar and Component Workshops
Active participation within Continuous Improvement / Lean initiatives.
Assist with metrics development supporting the wider BDUK QMS
Attend required meetings and present associated metrics for review

Preferred Skills, Qualifications, and Experience:

An understanding and previous experience of Quality Assurance Management
Aircraft maintenance experience
A basic Engineering Lifecycle knowledge
An experience in Aerospace / Defence background is highly desirable
Lead/ Internal Auditor AS9100 /ISO9001
Knowledge of MAA Regulations (MAOS, CAMO, CFAOS and DAOS)
Knowledge of Aerospace Standards (AS9110C / AS9100D)
An understanding / experience of conforming to the Defence Standards
Have a good understanding / application of Quality Management
Understanding / Appreciation of Continuous Improvement Techniques
Computer literate

Security Clearance: This position requires the ability to obtain a UK security clearance for which UK residency is required

The Boeing benefits package goes above and beyond, focusing on your physical, emotional, financial and social well-being. Here’s a snapshot of what we offer:

Competitive salary and annual incentive plans
Continuous learning - you’ll develop the approach and skills to navigate whatever comes next
Success as defined by you - we’ll provide the tools and flexibility, so you can make a meaningful impact, your way
Inclusive culture - you’ll be embraced for who you are and empowered to use your voice to help others find theirs
Excellent Adoption and Parental leave options
23 days plus UK public holidays and a Winter Break between Christmas and New Year
Pension Plan with up to 10% employer contribution
Company paid BUPA Medical Plan
Short Term Sickness: 100% pay for the first 26 weeks
Long Term Sickness: 66.67% of annual salary from 27th week
6x annual salary life insurance
Learning Together Programme to support your on-going personal and career development
Access to Boeing’s Well Being Programs, tool and incentives

Language Requirements:

Not Applicable

Education:

Not Applicable

Relocation:

Relocation assistance is not a negotiable benefit for this position.

Security Clearance:

This position requires the ability to obtain a security clearance post-start. See job description for details.

Visa Sponsorship:

Employer will not sponsor applicants for employment visa status.

Contingent Upon Award Program

This position is not contingent upon program award

Shift:

Not a Shift Worker (United Kingdom)","hiringOrganization":{"@type":"Organization","name":"Boeing","sameAs":"https://www.boeing.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"GBR - Wattisham Airfield, UK, United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":40,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-08-29","description":"

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

Quality Systems Specialist with experience in the pharmaceutical industry with:

Knowledge in Quality Systems and SOP.
Strong knowledge of relevant GMP, FDA, 21 CFR Part 11 and Data Integrity Regulations (Risk Assessment, Data Mapping, etc), EU regulations and the ability to interpret and apply them for intended use.
Proficient knowledge of computer systems (Microsoft Office etc.) with data collection software (database) and applications like Infinity and SAP.
Solid ability for analyzing data, detecting deviations, inconsistencies and interpret sampling test results.
Proficient knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe).

Qualifications

Bachelor’s degree in science (Chemical, Engineering, Biology, Pharmacy or Microbiology)
Six (6) years of experience in project management, investigations or relevant roles and responsibilities.
\nin the pharmaceutical industry.
Fully bilingual (Spanish/English) communication skills, both written and verbal.
Technical and scientific capability to make firm decisions and recommendations.
Microsoft Office, SAP, Infinity.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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\n\n

Summary

Join our growing QA team in a key role which provides Quality subject matter expertise (SME) and oversight to enhance our Quality Management Systems, thereby supporting global pharma in the production of life saving medicines and therapies. You will be responsible for ensuring that the QMS processes are efficiently maintained, and conform to internal and external client requirements, engaging cross functionally with exceptional SME team members to enhance our QMS and support our Client’s processes. The position is at the Castlebar, Co.Mayo facility and will report to the Senior Quality Engineer.

Essential Duties and Responsibilities

These include the following, others may be assigned to meet business needs.

Collaborate as a solution-oriented team member to work alongside the commercial and technical operations teams, delivering QA objectives to support business growth.
Track and report metrics and key performance indicators for the Quality Management System.
Collaborate with stakeholders to identify and support value-added improvements and key performance indicators.
Review and follow-up on open actions related to Corrective and Preventative Actions (CAPA), Out of Specification (OOS) reports and Deviations.
Support / host Client quality audits. Inclusive of addressing findings and required actions.
Management of the Internal Audit program including coordinating audit schedules, reviewing findings, tracking corrective actions, and providing insights and initiatives to drive continuous improvement.
Provide forward thinking innovative solutions and identify opportunities to add value to the teams’ deliverables.
Assist in the development of appropriate systems and processes to ensure delivery of information across functions to support enhanced performance culture.
Document Control - Site lead for managing Meissner SOPs and Document Control.
Manage quality training programs at Castlebar site to ensure these effectively mirror what is in place at HQ.
Site lead for training compliance to Meissner SOPs.
Other duties as required to support the growing Quality organization.

Qualifications, Education & Experience

The requirements listed below are representative of the knowledge, skill, and/or ability required to successfully function in this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Minimum 3 years of professional experience in the pharmaceutical industry in Quality Assurance focused role.
Team Oriented: Ability to integrate with the organizational Core Values, culture, and team climate.
Detail Oriented: Ability to focus on the details yet understand the overall direction.
Self-Motivated: Identifying what needs to be done and doing it before being asked or before the situation requires it.
Results Driven: The ability to focus on the desired result of one’s own or one’s unit’s work, setting challenging goals, focusing effort on the goals, and meeting or exceeding them.
Adept at multi-tasking and working in a fast-paced environment.
Strong, clear and concise communicator both internally and externally with pharmaceutical clients.
Bachelor’s degree in science, engineering or business preferred.
Willingness and availability to travel on company business.

Physical Demands

Occasional work may be done in an ISO Class 7 cleanroom environment. Powder free gloves, face masks, hairnets, gowns, and shoe covers must be worn. Because smokers continue to shed thousands of smoke particles even hours after smoking a cigarette and these particles will damage our products, only non-smokers are permitted to enter or work in the cleanroom. As a result, the successful candidate must be a nonsmoker.

Meissner is proud to be an Equal Opportunity Employer.

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Job Details

Job Location Sun Hydraulics 701 - Sarasota, FLPosition Type Full TimeTravel Percentage Up to 15%Job Shift DayJob Category QA - Quality Control

Description

Job Summary:

The Quality Systems Coordinator is responsible for implementing, evaluating, and maintaining the company’s quality system (QS) including documents and records.

Duties/Responsibilities:

Business Systems (Doc & Data Control) Coordinator (ISO, Safety, Environmental, etc.) \n
- Create or edit documents in company format.
- Request review and approval of new and revised QS documents.
- Prepare documentation and maintain records of compliance.
- Communicate QS document changes to affected employees.
- Support and harmonize best practice documents and procedures across multiple sites.
- Collaborate with teams to enhance operational efficiency and regulatory compliance.
- Maintain document records matrices of cross-references between QS documents with other criteria, such as training requirements, etc.
\n
Internal Audit Coordinator \n
- Create and maintain audit schedules for audit teams.
- Create and maintain associated audit documents, including improvement activities.
- Conduct internal audits (including Process, 5S, etc.).
\n
Customer Audit Coordinator \n
- Coordinate team and document schedules.
- Create and maintain associated customer audit documents.
\n
Management Review Coordinator \n
- Gather quality data. Interpret and report metrics to management or staff.
\n
Trainer support\n
- Conduct training classes (Quality management systems, and other operations).
- Train internal auditors.
\n
Perform other related duties as assigned.

Required Skills/Abilities:

Excellent verbal and written communication skills
Thorough understanding of quality standards, customer system requirements and methodology
Excellent organizational skills and attention to detail
The ability to work independently.
Managing time and multiple projects
Analytical and problem-solving skills
Leadership skills
Proficient with Microsoft Office Suite or related software
Knowledge of specific ISO standards
Experience in the development and improvement of quality management systems

Education and Experience:

2 years of college course work or equivalent
5 years of related business systems experience, 3 years manufacturing experience
ISO (or AS/ TS, etc.) Lead Auditor preferred

Physical Requirements:

The characteristics listed below are representative of the physical demands required by an individual to successfully perform the essential duties of this position. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential duties.

While performing the duties of this job, the employee is regularly required to stand, walk and sit; use hands to finger, handle, or feel; and reach with hands and arms
The employee is frequently required to talk and/or hear
Specific vision abilities required by this job include close vision, color vision, depth perception, and ability to adjust focus
This position may require travel to other Helios locations.

Work Environment:

The characteristics listed below are representative of the work environment typically encountered by an individual while performing the essential duties of this position. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential duties.

While performing the duties of this job, the employee is exposed to a normal office environment and occasional manufacturing environments.
Travel to other company locations may be required.

NOTE: The above stated duties are intended to outline those functions typically performed by individuals assigned to this classification. This description of duties is not intended to be all-inclusive nor to limit the discretionary authority of leadership to assign other tasks of a similar nature or level of responsibility.

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Come and join the leading #avoexperts 🥑

Westfalia Fruit is a leading multinational supplier of fresh fruit and related value-added products to global markets. Through our vertically-integrated supply chain we grow, source, ripen, pack, process and market quality avocadoes & fresh produce – 365 days a year & across the globe.

With the largest avocado-growing footprint in the world, we are recognised as the leading #avoexperts and considered as the supplier of choice to both retail & wholesale customers whom we serve from sales offices in the UK, Europe, North America, Latin America & Southern Africa.

We’re looking for two Quality Systems Support professionals to join our new team in, Spalding, UK.

Role Summary

The Quality Systems Support provides administrative and coordination support to ensure the effective running of the Quality Management System (QMS). The role focuses on document control, policy and procedure updates, coordination of the internal audit schedule, and supporting the closure of non-conformances across all sites and departments.

This position plays an essential role in maintaining compliance with food safety, legal, and customer standards, while supporting the Quality Systems Manager in embedding a culture of continuous improvement and operational efficiency across the business.

Travel Requirements

Occasional travel to other UK sites to support audits or document reviews will be required.

Responsibilities include:

Keep Quality Systems Sharp – Maintain and update QMS documentation to ensure policies and procedures are always current, compliant, and accessible.
Champion Policy Rollouts – Support the implementation of new and updated policies across all business areas.
Master of Document Control – Manage version control, archiving, and ensure seamless document accessibility in line with company standards.
Lead Internal Audits – Coordinate and maintain a robust internal audit schedule across all sites, ensuring timely execution and trained auditors.
Drive Compliance & Closure – Track audit findings, support departments with non-conformance resolutions, and provide regular status updates.
Support Third-Party Success – Assist in preparing for external audits and certifications including BRC, GlobalG.A.P, and key customer standards.
Promote Continuous Improvement – Help monitor site KPIs, support improvement actions, and maintain detailed performance records.
Coach & Guide – Train internal auditors and teams on audit techniques, documentation standards, and best practices for compliance.
Communicate with Impact – Share audit outcomes, system updates, and ensure quality records are accurate and audit-ready at all times.
Work Across the Business – Collaborate with internal departments and external partners like certification bodies and service providers.

Requirements

Experience we look for:

Essential

A-levels or equivalent required.
HACCP Level 3 or willingness to complete.
Experience managing documents and systems in a regulated environment.
Strong IT and data management skills (Excel, Word, document management systems).
Good organisational skills with attention to detail.
Proactive and well-organised, able to manage multiple priorities.
Strong communication skills and ability to work across functions.
Detail-oriented with a methodical approach.
Team player with a willingness to learn and develop.

Desirable

Further training in Food Safety, Auditing, or Quality Management desirable.
Previous administrative or technical support experience in food manufacturing, FMCG, or fresh produce preferred.
Exposure to audits (internal or external) desirable.
Knowledge of food safety standards (HACCP, BRC, GMP) desirable.
Experience in fresh produce, food manufacturing, or FMCG environment.
Familiarity with BRCGS or customer technical standards.
Training in internal auditing or document control systems.
Continuous improvement mindset and interest in developing a career in Quality.

Benefits

What can Westfalia Fruit offer you?

20 days holidays
Free on-site parking
Additional Annual Leave day on your Birthday
Company pension plan
Medicash plan
Life Insurance

Please note that this position does not have a specific closing date. We encourage you to apply as soon as possible as we will be reviewing applications on a rolling basis and the advert may be removed at any time.

We’re an equal opportunity employer. All applicants will be considered for employment without attention to age, ethnicity, religion, sex, sexual orientation, gender identity, family or parental status, national origin, or veteran, neurodiversity or disability status.

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Come and join the leading #avoexperts 🥑

We’re looking for a Quality Systems Manager to join our team in, Spalding, UK.

The Quality Systems Manager is responsible for maintaining and improving the UK site-level Quality Management System (QMS), ensuring compliance with food safety, legal, and customer standards. The role supports the development of the HACCP/Food Safety and Quality Plan, manages internal and third-party audits, and embeds a strong culture of compliance, food safety, and continuous improvement.

This position plays a critical role in safeguarding product integrity, supporting customer satisfaction, and enabling operational efficiency by ensuring systems, documentation, and processes are robust, effective, and consistently applied.

Travel Requirements

Occasional UK travel to suppliers, service providers, or industry bodies for audits, training, or system alignment.
Limited international travel may be required to support alignment with global systems.

Responsibilities include:

Lead the Quality Standard – Own and maintain a fully functional Quality Management System (QMS), ensuring full compliance with all legal, customer, and industry standards.
Champion Food Safety – Drive the ongoing development of HACCP and Food Safety & Quality Plans, embedding a strong food safety culture across site operations.
Audit-Ready, Always – Manage internal audit schedules, lead corrective and preventive actions, and ensure the site is always prepared for external certifications like BRC and GG COC.
Train & Empower Teams – Deliver impactful training on QMS, GMP, and food safety practices to build knowledge and accountability across the workforce.
Drive Compliance Metrics – Track and deliver key site KPIs for audits, hygiene, GMP, and environmental standards, ensuring continuous performance improvement.
Control Hygiene & Pest Management – Oversee hygiene service providers and pest control contractors to maintain the highest site standards.
Cross-Functional Collaboration – Work closely with Operations, Technical, Hygiene, and Engineering teams to enhance processes and ensure quality at every stage.
Support Continuous Improvement – Be a key player in site improvement initiatives, evolving systems to meet changing business and regulatory demands.
Right First Time Approach – Champion grading and defect management at source to reduce waste and increase product quality from the ground up.
Key Liaison Point – Act as the main contact for third-party auditors, industry bodies, and certification organizations to represent the site professionally and confidently.

Requirements

Experience we look for:

Essential

Experience in a quality systems role within fresh produce, FMCG, or food manufacturing.
Demonstrable experience managing QMS, audits, and certification processes.
Strong working knowledge of UK food safety legislation and retailer standards.
Proficient in HACCP, GMP, and internal auditing practices.
Experience with QMS platforms and data-driven quality management.
Ability to interpret and apply standards from BRC, GlobalG.A.P, and customer codes of practice.
Detail-oriented and systematic, with strong organisational skills.
Confident communicator able to influence at all levels.
Problem-solver with a continuous improvement mindset.
Collaborative team player with a proactive, hands-on approach.

Desirable

Food Safety or Quality Management qualifications (HACCP, Lead Auditor, BRC) preferred.
Experience working with fresh produce, ripening, or packing operations.
Exposure to digital quality systems, traceability tools, and data analytics platforms.
Continuous improvement certification (Lean Six Sigma, Kaizen).
Prior engagement with UK retailer audits and customer quality requirements.

Benefits

What can Westfalia Fruit offer you?

20 days holiday plus public holidays
Free on-site parking
Additional Annual Leave day on your Birthday
Company pension plan
Medicash plan
Life Insurance

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About This Role

As a Quality Systems Manager, you will be accountable for the implementation, effectiveness and oversight of the governance, risk and compliance of the overall quality management and compliance management systems.

The role ensures data and document control functions effectively and efficiently. Also inherent to this role will be providing expert guidance and advice in relation to all aspects of ISO standards, regulatory requirements, and compliance.

This role will be hired initially as a 2-year fixed term contract.

The role we are offering you

Define and manage audit & compliance programs and schedules
Review and evaluate project deliverables from all phases of the lifecycle to provide an independent technical review
Identify, drive or manage Continual Improvement and Operational Excellence programs
Systematically monitor and manage the quality management systems, their use, compliance and meeting legislative & regulatory requirements

Our ideal candidate has:

Extensive understanding of ISO 9001 (and others), ASDEFCON and WHS regulations
Proven experience managing Quality Management Systems
Experience with Microsoft Office Suite
People leadership experience

Location:

This role will be ideally based at either Homebush, NSW - we may consider Brisbane, QLD
We operate a hybrid working approach.
Your role will involve some national and international travel

What CAE offers you:

Opportunity to make a positive impact on Australian defence and security
Exciting career paths in a truly global business
Access to a generous ADF Reserve Service Policy

Security requirements

As the Australian Department of Defence is a major client, you must be eligible for SECRET (NV1) level Defence security clearance, and preferably already hold a current SECRET (NV1) clearance.

Applications

If this role fits what you are looking for and you believe you have the necessary skills and experience, click ‘Apply Now’ and attach your resume.

Read our FY24 Annual Activity and Corporate Social Responsibility Report

Instagram: www.instagram.com/CAE_inc

#LI-AL2 #CAE #CAEpilot #CAErecruiting

Position Type

Temporary (Fixed Term)

CAE thanks all applicants for their interest. However, only those whose background and experience match the requirements of the role will be contacted.

Equal Opportunity Employer

CAE is an equal opportunity employer committed to providing equal employment opportunities to all applicants and employees without regard to race, nationality, colour, religion, sex, gender indentity and expression, sexual orientation, disability, neurodiversity, veteran status, age, or other characteristics protected by local laws.

If you don't see yourself fully reflected in every job requirement listed in the job posting, we still encourage you to reach out and apply. At CAE, everyone is welcome to contribute to our success. Applicants needing reasonable accommodations should contact their recruiter at any point in the recruitment process. If you need assistance to submit your application because of incompatible assistive technology or a disability, please contact us at CAECarrieres-Careers@cae.com

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Director Quality Systems

Are you excited by quality and compliance within the Medical Device industry? Are you a passionate people manager, keen to make your team grow and bloom? Do you want to be part of a pioneering Quality Management team, continuously setting the bar high in everything we do?

Then this might be your defining moment. Apply today and join us as Director of Global Quality Management Systems out of our HQ in Ballerup, Denmark or Augsburg, Germany.

Key responsibilities

In this role, you will lead a stellar team consisting of 10 talented QM (senior) professionals. Together, you will ensure quality and regulatory compliance of Ambu products and processes across the organization by continuously monitoring compliance.

This will include development and optimization of the Quality Management System and Processes within your team’s area of responsibility. Moreover, you will be accountable for the Audit Management globally.

Your main responsibilities will include:

Daily manager of the Department Global QM Systems in Ambu
Ensure a smooth change control process which is in compliance with regulatory requirements
Implement effective global processes, with optimal balance between global and local responsibility
Ensure a high degree of scalability, which means that the process of adding (or removing) sites covered by the Quality System can be done with a minimum of changes to the existing QMS
Overall responsible for Global QMS Expert Forum, that identify and coordinate proactive solutions to global challenges to Ambu Quality Systems.
Ensure monitoring of Global QMS system to ensure continued compliance and efficiency - and act when non-conformities are identified
Ensure know-how center for quality management system issues, and ensure proper implementation through education and assistance to the organization
Educate the organization on the importance of QM
Ensure Internal Audit Plans and Corporate Audit Plans are executed, manage and participate in internal audit (audit coordination)
Planning and leading of External audits. Contact to external auditors.
Host and participate during inspections from authorities. Overall responsible for Corporate Quality Systems participation in Audits.
Project management of selected projects within QMS area including integration and partnerships Global sales organization

Suggested candidate profile

Skills and experiences can be earned in many different ways, and we understand that the best fit for the role cannot be prescribed on paper. You are however likely to succeed in this position if you:

Havea relevant academic background, BSc / MSc or higher
Have at least 8-10 years’ experience of leading a quality organization within Medical Devices
Have strong knowledge of relevant regulations for medical devices e.g., ISO13485, EU MDR, MDSAP, UK MD
Have a passion for quality and focus on QM business partnering with the organization

Ambu – a visionary and international workplace where your efforts matter

Ambu is a company that expands rapidly and has ambitious growth targets. We meet these targets through interdisciplinary teamwork between motivated and highly skilled employees. Your contributions and efforts are crucial to our success and by joining us you will get the opportunity to work in an international head office with an informal working environment.

We offer great opportunities for personal development. Furthermore, we offer a wide range of professional, social and financial employee benefits in addition to exciting job challenges and continuous professional and personal development

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Job Purpose

Responsible for overseeing, assisting to develop, implementing and maintaining a Quality and Food Safety Program that ensures all products are within specifications and meet all food safety and quality requirements.

Skills and Qualifications

General Qualifications include, but are not limited to:

Shall have attended a Chemical Safety Training session within the past 12 months.
1. Shall have attended GMP, FSMA, Food Defense Awareness, and Allergen Training.
2. Shall meet all requirements of the SQF Program.
3. Shall meet all requirements of the FSMA Preventive Controls program. Including obtaining PCQI training and intentional adulteration training.
4. Shall comply with all GMP Requirements
5. Shall comply with all requirements for Personal Protective Equipment as defined by appropriate plant procedures.
6. Shall comply with all Safety Rules and Policies.

Duties and Responsibilities

Quality Assurance Responsibilities include, but are not limited to:

Responsible for compliance with regulatory, food safety, food quality, and customer requirements.
Act as a primary PCQI for daily paperwork signoff once training is complete
Manage and Oversee the TraceGains program for the facility
Work in conjunction with procurement manager to obtain necessary documentation for the supplier approval program for all incoming ingredients and packaging
Editing and Implementing of new and existing SOPs as needed.
Maintain laboratory supply inventory and order as needed.
Site Liaison to Ecolab Chemical Account Representative for SSOP validations
Oversight of all equipment calibration certification evidence in the facility (ex. Scales, thermometers, Ph Meter, etc.)
Validate completion and effectiveness of all corrective actions, CAPAs, and RCAs in the facility
Work in conjunction with Sanitation Management to ensure Master Sanitation is in compliance.
Ensure the plant programs comply with government regulations regarding quality control and coordinate activities related to visits from regulatory agencies and/or third part auditors.
Assist QA Manager with any additional tasks
In the event of the QA Assistant’s absence, the Plant Manager shall assign these responsibilities.

Prairie Farms Dairy, Inc. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

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We are looking for a talented Quality Systems Specialist to join our team in Pandan Ave, Singapore. This will be following Onsite work model.

Acts as an extension of senior management ensuring a positive customer experience while being the representative of senior management to others. Provides administrative support and performs numerous duties, including scheduling, writing correspondence, emailing, overseeing visitors, routing callers and answering questions and requests.

In this role, you will make an impact in the following ways:

Key responsibilities:

Anticipates to the needs of senior management and manages his/her schedules. Arranges and coordinates travel arrangements including expense reports and visa/passport requirements.
Gathers, compiles, verifies and analyses information for management' use in documents such as memos, letters, reports, speeches, presentations and news releases.
Facilitates smooth communications between senior management and coworkers and between senior management and external parties such as media, customers, vendors and the public. Maintains the security and confidentiality of management' records and files.
Monitors, reviews and approves standard expenditures to ensure the activities of the office are conducted within established budgets.
Reports required information on a regular basis as assigned (e.g. monthly).
Performs various tasks using independent judgement and discretion; e.g., preparing documents and presentation materials; screening and responding to incoming correspondence, inquiries, and phone calls; drafting letters and official information releases; arranging and attending meetings; taking and distributing minutes.
Act as formal resource for colleagues with less experience.
Completes other activities for senior management upon request and/or as required.

To be successful in this role you will need the following:

Values differences - Recognizing the value that different perspectives and cultures bring to an organization.
Action oriented - Taking on new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
Communicates effectively - Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences.
Customer focus - Building strong customer relationships and delivering customer-centric solutions.
Ensures accountability - Holding self and others accountable to meet commitments.
Plans and aligns - Planning and prioritizing work to meet commitments aligned with organizational goals.
Data Analytics - Discovers, interprets and communicates qualitative and quantitative data; determines conclusions relying on knowledge of business or functional frameworks; simultaneously applies statistics, data validity, data visualization, and problem-solving approaches to effectively extract meaningful patterns and business insights; presents conclusions and outcomes that enable data driven business decisions.
Data Communication and Visualization - Constructs a tale of the business problem, root cause, solution options, and opportunities through illustrating data visually, including reports and dashboards.

Preferred Qualification:

High school diploma or certificate of completion of secondary education or equivalent experience to the extent such experience meets applicable regulations.
This position may require licensing for compliance with export controls or sanctions regulations.
Significant work experience and in-depth knowledge obtained through specialized training and relevant experience.
1. Supports the Quality Systems Manager with compliance by ensuring company policies, processes and standards are effectively implemented.
2. Leads the planning and completion of ISO 9001 internal audits for the site. Gathers and analyzes data from internal audit findings to make recommendations to leadership team on improving the Quality Management System.
3. Engage with Global NRP QA Corp team to lead changes needed for the site. Supports collection and/or calculation of input metrics related to the quality system, scorecards for the Corp.
4. Key administrator for CQMS and Document Management System. Supports the key business processes documentation and maintenance, entry of documentation and identifies problems needing addressed, including follow up on overdue approvals, reviews, ownership changes, etc. Helps maintain the quality system documents prescribing the quality management system, the documented procedures or reference to them, and a description of the interactions between the processes of the management system.
5. Engages in preparation and analysis for Quality Management reviews (including but not only customer satisfaction), communicates and maintains follow-up actions.
6. Provides information as necessary to external auditors or certification bodies, complying with content, timing, and format requirements.
7. Delivers/Facilitates specific quality systems related education, e.g., application user training, internal auditor training)
8. Responsible for applicable systems related to plant customer issues such as corrective action requests, supplier corrective action requests, nonconforming material reports, etc.
9. Conduct of SOX audits and driving corrective actions from our GSCS team for any non-conformities to claims processing found.
10. Co-administrator for SMARTLPA system and lead for changes/updates on process audits.

\nCummins is an equal opportunity employer. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, sex, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity, or other status protected by law.","hiringOrganization":{"@type":"Organization","name":"Cummins","sameAs":"https://www.cummins.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Singapore, Singapore, Singapore","addressCountry":"Singapore","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":49,"item":{"@type":"JobPosting","title":"Quality Systems Engineer","datePosted":"2025-09-02","description":"

Company Description

Located 70 km from Mexico City, Bosch Plant in Toluca (TlP) has manufactured since 1966 a wide range of products for the Mobility Business for Electrified Motion (EM), Power Solutions (PS) and Mobility Aftermarket (MA) Divisions.

\nOur vision: Be the plant of choice for customers, stakeholders and associates.

Job Description

Main Objective:

Implement and support quality tools (SPC, MSA, PPAP, AMEF, 14QP and Problem Solving), ensuring compliance with specific customer requirements and BOSCH Quality System

What challenges will you have?

Plans and executes internal process audits in accordance with the VDA 6.3 standard.
Effectively implements quality tools at the locations (including Core Tools, 14QP, problem solving, audits, LPCs, etc.).
Ensures compliance with IATF 16949 and customer-specific requirements by supporting internal and external system audits and ensuring proper implementation within the Bosch quality system.

Qualifications

Who are we looking for?

At least 3 years of experience in Automotive Industry
Advance English Level is required
We value Critical Thinking and Negotiations skills

Technical Knowledge

Knowledge on Problem Solving methodologies
Experience with Quality Standards, Regulations and Customer Requirements (OEM’s)
Solid Data Analysis skills

Additional Information

Bosch is constantly expanding its international presence, since for us cultural diversity represents one of our greatest strengths. We are continuously promoting the growth of our more than 17,000 associates, who develop their full potential in one of the highest quality companies in technology. We value the balance between personal and work life as one of the main tools to improve the creativity and productivity of our associates.

","hiringOrganization":{"@type":"Organization","name":"Bosch Group","sameAs":"https://www.bosch.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Toluca de Lerdo, Méx., Mexico","addressCountry":"Mexico","addressRegion":"North America"}}}},{"@type":"ListItem","position":50,"item":{"@type":"JobPosting","title":"Quality Systems Specialist","datePosted":"2025-09-02","description":"

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose

The Quality Systems Specialist is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.

Responsibilities

Assist with proper integration and support of quality regulations: drug, biologics, device and/or combination products.
Assist project teams in planning, preparation, review and approval of quality documentation.
Complete and route change requests for process document creation, maintenance, and implementation.
Create quality system documentation and specifications with guidance from technical teams following approved templates and guidelines.
Assist with or co-lead audits of documentation, facilities and equipment.
Assist in the design of effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality system.
Perform assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within our quality system.
Participate in training and education programs for various aspects of quality assurance.

Qualifications

Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred.
3+ years’ experience in quality assurance, quality oversight or relevant experience.
Technical knowledge in as many of the following areas as possible: Quality, Regulatory, Process Sciences, Manufacturing Operations.
Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products preferred.
Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products preferred.
Experience working in both team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
Strong oral and written communication skills needed.
Excellent interpersonal skills a plus.
Runs small projects to deliver tactical results.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
This job is eligible to participate in our long-term incentive programs

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

","hiringOrganization":{"@type":"Organization","name":"AbbVie","sameAs":"https://www.abbvie.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mettawa, IL, United States","addressCountry":"United States","addressRegion":"North America"}}}}]}

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