QC Reviewer - Eurofins BioPharma Product Testing Toronto Inc.

Company Description Eurofins Scientific is an international network of independent life sciences companies, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 57 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. The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades. Job Description Review of all laboratory related documents in the Quality Control Laboratory e.g: finished products, bulk, raw material and stability study products as per GMP requirements in a timely manner as per the agreed timelines. Review accuracy of data entries in raw data and chromatographic data management systems prior to release of the CoA in eLIMS. To ensure data integrity is maintained in all the process. Complete all training assignments and maintain personal training records. Participate in and/or lead Out of specifications Investigations OOS. Complete Corrective and Preventive Actions (CAPA’s). Participate in Internal, Customer and Regulatory Audits. Assist laboratory personnel with documentation issues and provides coaching and guidance to Quality Control team. Provide support for Regulatory Inspections. Identifies and implements key process improvements to areas to enhance systems, gain site efficiencies and elevate GMP requirements. Notifies department supervisor/manager regarding omissions, incomplete testing results or other irregularities. Ensures the test methods, protocols and Standard Operating Procedures (SOPs) have been followed by the scientists/chemists during the testing. May be essential to perform alternating or rotating shift work (as required). Follows up with analysts/technicians to ensure that all necessary corrections are corrected in accordance with Good Manufacturing Practices standards. Audits calibration related documents and other QC documents; Inputs data for trending departmental KPIs. Qualifications Bachelor of Science degree (or equivalent combination of education and experience such as College with 5-10 years of pharmaceutical QC testing/records review experience) in Chemistry, Biochemistry or related biological science or equivalent in job experience. Over 2 years of experience working in a pharmaceutical regulated Laboratory environment or Pharmaceutical Company. Ability to work with electronic systems (eg. LIMS) and other lab equipment to be able to perform audit trail of testing records. Knowledge of GC, HPLC, UV, IR, ICP-MS/OES and other analytical instrument. Sound knowledge of Health Canada and FDA regulations. Works well under pressure. Quality Assurance /Quality control audit background in pharmaceutical industry is an asset Extended hours or weekend work may be required from time to time. Excellent language, writing and communication skills required. Additional Information The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. Please note that relocation to Mississauga, ON is expected in 2026. 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 This posting is supported by AI technology to assist in screening candidates and resumes. This posting is for a current vacancy and the successful candidate will start as soon as possible. Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process. NO AGENCIES, CALLS OR EMAILS PLEASE Compensation: CAD 50000 - CAD 60000 - yearly

The QC Reviewer is responsible for reviewing laboratory documentation, including finished products and stability studies, to ensure compliance with GMP requirements. They also participate in OOS investigations, CAPA processes, and provide guidance to the Quality Control team during audits.

Candidates must hold a Bachelor of Science degree in Chemistry, Biochemistry, or a related field, along with at least 2 years of experience in a pharmaceutical regulated laboratory. Proficiency in analytical instruments like HPLC and GC, as well as knowledge of Health Canada and FDA regulations, is required.

• Health coverage • Dental coverage • Life insurance • Disability insurance • RRSP with 3% company match • Paid holidays • Paid time off

• Quality ControlPreferred

Identified from the job description. Confirm important requirements above.

• Quality control
• GMP
• Data integrity
• Chromatographic data management
• OOS investigations
• CAPA
• Regulatory audits
• LIMS
• GC
• HPLC
• UV
• IR
• ICP-MS
• Health Canada regulations
• FDA regulations
• Documentation review
• Training Records Management
• In Vitro Diagnostics
• FDA Regulations
• Laboratory Equipment
• Analytical Testing
• Time Off Management
• Analytical Method
• Shift Work
• Research
• Artificial Intelligence
• Chemistry
• Auditing
• Biochemistry
• Biology
• Biological Materials
• Good Manufacturing Practices
• Calibration
• Corrective And Preventive Action (CAPA)
• Clinical Trials
• Communication
• Cosmetics
• Data Integrity
• Data Management
• Standard Operating Procedure
• Genomics
• High-Performance Liquid Chromatography
• Key Performance Indicators (KPIs)
• Laboratory Information Management Systems
• Life Sciences
• Pharmaceuticals
• Quality Assurance
• Coaching
• Test Method
• Writing

• Science & Research
• Healthcare
• Manufacturing
• Quality Control Reviewer
• Quality Assurance Specialist
• Product Graders and Testers (except Foods and Beverages)
• Inspectors, Testers, Sorters, Samplers, and Weighers

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Posting language

English

Working hours

40 hours per week