QC Reviewer - BioPharma Product Testing Inc.
- Full-time
- Compensation: CAD 50000 - CAD 60000 - yearly
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 Laboratorye.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.
- 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…
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