Chemistry Analyst I - Eurofins BioPharma Product Testing

  • Toronto, ON, Canada
  • Full-time

Company Description

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 just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing.  

In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years

Job Description

Basic Function: The Analyst I will be responsible for performing routine analysis in support of Quality Control department and GMP operations. Primary responsibilities will include prepare reagents, standards and sample to perform release testing under minimum supervision of Laboratory Manager.

Key Responsibilities:

•             Analyze API, Raw Materials and Finished products for Assay, Impurities & Dissolution study using  HPLC instrument with minimum supervision;

•             Ensure all work is performed in compliance with applicable SOP’s, cGMP’s, and GLP’s.

•             Recognizes OOS or out of trend results and assist laboratory manager in the completion of lab investigations.

•             Review technical data, documents, and proposals as required.

•             Troubleshoot technical issues/ difficulties with methods.

•             Prepare mobile phase and solution to perform analytical testing.

•             Co-ordinate with team members to perform method transfers between R&D group to QC group;

•             Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.

•             Other duties as assigned by Laboratory manager.



•             Bachelor of Science in Chemistry, or related pharmaceutical discipline.

•             Minimum 1 to 3 years of experience in Pharmaceutical QC environment.

•             Ability to troubleshoot and resolve issues.

•             In-depth understanding of chromatography principles, types and techniques.

•             Must possess strong communication skills, both written and verbal.

•             High level of accuracy and attention to detail.

•             Proficient in Microsoft office programs (Outlook, Word, and Excel).

•             Working knowledge of  GC, UV, FT-IR, KF, titrations and dissolution instrument would be an asset

•             Hands on experience with pharmaceutical

Additional Information

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 at

We thank all applicants for showing an interest in this position. Only those selected for an interview will be contacted. NO AGENCIES, PHONECALLS OR EMAILS PLEASE


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