Product Analyst (m/w/d)

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. Reporting directly to the Department Head - Chemistry, the Analyst will be responsible for providing basic technical support and analysis within the Biopharmaceutical Chemistry Testing Laboratory. This is a deadline-based, high-pressure work environment with on-going projects for a variety of clients.
The Analyst will have over 5 to 10 years of laboratory testing experience with demonstrated ability to complete more complex role/duties. Has handled variety of instrumentation for analytical testing and will be able to work independently with minimal/no supervision. The incumbent must be energetic, exceedingly well-organized, flexible, and must have the ability to interact with customers and staff in a fast-paced environment, sometimes under pressure, while remaining proactive, resourceful, and efficient. Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
Analyze API, Raw Materials and Finished products for Assay, Impurities & Dissolution study using HPLC /GC instrument with minimum supervision.
Review technical data, documents, and proposals as required.
Proficient in Microsoft office programs (Outlook, Word, and Excel).
Hands-on experience with pharmaceutical data acquisition software e.g. Troubleshoot technical issues/ difficulties with methods.
Coordinate with team members to perform method transfers between R&D group to QC group.
Strong interpretation of routine analysis or tests.
In-depth understanding of chromatography principles, types and techniques.
Be able to work under GMP guidelines, and be proficient with USP and pharmaceutical testing.
Explaining latest, applicable methods and techniques to perform various experiments and teaching necessary techniques that need to be adopted to complete a particular experiment or an allotted assignment.
Accountable for the integrity and traceability of all data generated and reported.
Design, preparation, and production of study materials including procedure manuals.
Using a wide range of sophisticated equipment and instruments to conduct analysis and research and troubleshoot instrumentation/methods.
Perform other departmental tasks such as cleaning, supply ordering, assist with instrumentation training and maintenance, etc.
Perform analytical tests utilizing HPLC/UPLC, GC, UV, IR, FTIR, KF and other laboratory instruments.
Assess, compare and perform risk assessments for compendial method compliance according to USP, EP, and other regulations.
Mentoring/training junior staff members and Imparting training to new recruits for operation, calibration and preventive maintenance of GCMS/GC/HPLC/ LC-MS/MS, etc .
Writing SOPs.
Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method.
A solid background and understanding of Chemistry is mandatory
Computer proficiency- Microsoft Office , especially Excel
Experience working in contract Laboratory considered an asset.
~ Experience working with Pharmaceuticals.

Please note that this role will require relocation to the Company’s Mississauga office following our planned office move in 2026.

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 at