Data Reviewer - Eurofins Experchem Laboratories, Inc.

Company Description

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

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

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

Job Description

Eurofins Experchem Laboratories, Inc. is seeking a detail-oriented and analytical Data Reviewer to join our team in Toronto, Canada. In this role, you will be responsible for ensuring the accuracy and integrity of laboratory data, supporting our commitment to delivering high-quality analytical services to our clients.

• Review and validate laboratory data for accuracy, completeness, and compliance with protocols, SOPs, GMP, and regulatory requirements.
• Identify and investigate data discrepancies, anomalies, or trends, and propose/carry out corrective actions as needed.
• Collaborate with laboratory personnel and liaise with other departments to resolve data-related issues, verify appropriate methods and specifications, and improve overall data quality.
• Maintain detailed documentation of all data review processes, investigations, and findings.
• Perform data review and approval for method validation, method verification, and method transfer projects; organize and finalize validation packages for clients.
• Review and approve calibration, preventive maintenance data, and Instrument/Equipment Qualification protocols and reports.
• Ensure timely completion of corrections and prompt data release.
• Verify that all results are within specification; notify appropriate parties of any out-of-specification (OOS) results and apply sound judgment during investigations.
• Troubleshoot issues quickly and effectively, ensuring method compliance or appropriate method modifications.
• Apply and enforce data integrity procedures and ensure adherence to internal SOPs and GMP regulations.
• Prepare comprehensive reports summarizing data review findings and recommendations.
• Support the development and implementation of improved data review procedures and quality control measures.
• Participate in internal and external audits related to data integrity and quality assurance.
• Act as delegate for the Supervisor in sending results to clients, when required.
• Stay up to date with industry standards, regulatory requirements, and best practices in data management and quality control.
• Perform other duties as assigned by the supervisor.

Qualifications

• Bachelor's degree in Chemistry, Biology, or a related scientific field.
• Proven experience in data review or quality assurance (QA) within a laboratory setting.
• Previous experience with Laboratory Information Management Systems (LIMS) and a solid understanding of laboratory processes, analytical methods, and instrumentation.
• In-depth knowledge of quality control procedures, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory requirements in the pharmaceutical or chemical industry.
• Strong proficiency in data analysis and statistical software such as Excel, SPSS, R, or SAS.
• Exceptional computer skills, particularly with MS Office (Outlook, Word, Excel).
• Excellent attention to detail, high level of accuracy, and strong analytical and organizational skills.
• Ability to manage multiple priorities, multitask, and remain calm under pressure in a fast-paced environment.
• Strong written and verbal communication skills.
• Ability to work independently while effectively contributing to a collaborative, team-based environment.
• High level of professionalism, maturity, sound judgment, and discretion, especially when handling confidential information.
• Proactive, self-disciplined, and able to demonstrate a high level of productivity.
• Demonstrated satisfactory work performance and attendance record.
• Willingness to learn quickly and apply new knowledge across different scenarios.
• Relevant certifications in data analysis or quality control (preferred).

Additional Information

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

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