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. Under the direction of Department Head of R&D;, LCMSMS analyst would be responsible for supporting the department analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory that meets the departmental goal.

Perform Method

Development, Method Validation, Method Transfer and Routine Analysis using LCMSMS and other instrumentation techniques. Reviewing data, preparing protocol and report to ensure R&D; projects meet the timeline. Troubleshoot technical issues/ difficulties with all tests related with Analytical Laboratory.

Manage multiple research projects simultaneously to meet the project timeline. Verify that all study materials (including standards, reagents and columns) are in stock.



Understand and follow Quality System documents relevant to responsibilities, e.g.

Quality

Manual, SOPs, GMP/GLP/USP and Methods. Adhere to appropriate quality measures to meet or exceed the standards set by GMP government regulatory and company requirements relevant to assigned duties. Maintaining a neat and accurate record system of daily activities related with all R&D; and Quality Control testing.

Guide, mentor and train junior staff members to achieve expected quality and TAT metrics. A minimum of 3-5 years working experience in the Pharmaceutical/Biopharmaceutical field, in a GMP environment. Strong experience with Method Development, Method Validation, Method Transfers study.

Computer proficiency-MS Office (Outlook, Word, Excel), LIMS, Empower & Analyst Software in a GMP environment. HPLC-PDA & GCMSMS experience would be an asset. Bachelor of Science in Chemistry, or diploma in related field.

A solid background of Mass Spectrometry is mandatory. Please note that this role will require relocation to the Company’s Mississauga office following a planned office move in 2026. This position will be working in a laboratory workplace where standing is required for greater than 50% of the time to work at the bench for analyses.

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

📌 Full Time - Analyst (Toronto)
🏢 Eurofins
📍 Toronto