QA Data Reviewer - Eurofins BioPharma Product Testing Toronto, Inc

Eurofins View all jobs

  • Toronto, ON
  • $50,000 per year
  • Permanent
  • Full-time
  • 23 days ago
  • Apply easily
Company DescriptionEurofins 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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionThe Quality Assurance Data Reviewer is a position reporting to the QA Director and is responsible for ensuring the compliance with applicable regulations (i.e. GMP, Health Canada and FDA regulations), for clients requiring quality assurance services.Responsibilities:
  • Perform data review of batches carried out in laboratory, including raw data review and calculations;
  • Perform data review of method validation and method transfer projects as well as organize final validation packages for clients;
  • Perform data review of local Method Development and/or Verification Reports;
  • Prepare/Review/Check Instrument/Equipment Qualification protocols and reports;
  • Review and approve calibrations and preventative maintenance;
  • Ensure GMP compliance;
  • Apply and follow the data integrity procedures;
  • Ensure reports follow designated SOPs and comply with GMP;
  • Ensure corrections are completed in a timely manner and released promptly as required;
  • Ensure appropriate analyses conducted and proper method followed, and method modifications are applied and followed;
  • Verify that all results reported are within specification;
  • Display proper judgment during investigations;
  • Troubleshoot and respond quickly when problems arise;
  • Any other duties assigned by Supervisor.
Qualifications
  • Bachelor of Science in Chemistry, Microbiology, Food Science or Life Science;
  • Minimum 3 years of GMP experience reviewing chemical analytical reports is required;
  • Hands-on experience reviewing HPLC, GC, UV, and wet chemistry data;
  • Knowledge of GMP requirements;
  • Must speak and write English fluently;
  • Exceptional computer skills with a high level of competence with MS Office (Outlook, Word, Excel);
  • Must possess excellent communication skills, both written and verbal;
  • Excellent organizational skills;
  • High level of accuracy and strong attention to detail;
  • Ability to work independently, while supporting a collaborative, team-based department;
  • Ability to multitask and remain calm under pressure;
  • High level of professionalism, maturity, good judgment, and discretion when dealing in confidential matters;
  • Must be proactive, self-disciplined, and able to demonstrate a high level of productivity;
  • Demonstrate satisfactory work performance and attendance record;
  • Willingness to learn with the ability to retain information quickly and apply knowledge to various scenarios.
  • Previous experience in QA is essential.
Please note that this role will require relocation to the Company’s Mississauga office following our planned office move in 2026.WORKING CONDITIONS:
  • This position will be working in a laboratory environment where standing is required for greater than 50% of the time. Light lifting requirements of no more than 30 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE.
  • Shift work and overtime may be required, as well as working periodic weekends and/or evenings.
Additional InformationPlease note that relocation to Mississauga, ON is expected in mid-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 .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 atWe 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.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

Eurofins