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R&D Analytical Chemist – Eurofins BioPharma

Eurofins NSC Canada Inc

This is a Full-time position in East York, ON posted February 21, 2021.

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 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description Basic Function: Under the direction of the Department Head, the R&D Analyst will be responsible for supporting the research and development department through coordinating research activities directed toward the development of new methods and conducting validations that meet department revenue and profit growth and expense objectives.

The position is instrumental in the development of methods and R&D processes/procedures for GMP compliance as well as maintaining operational efficiencies.

Key Responsibilities : Develop & validate assay and Impurities method using HPLC & GC with minimum supervision; Write R&D, Method Validation, Method Transfer protocols and reports; 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; Other tasks as assigned by supervisor.

Qualifications Qualifications: Bachelor of Science in Chemistry, or related pharmaceutical discipline; Minimum 2 to 3 years of experience in Pharmaceutical R&D environment; Must possess excellent communication skills, both written and verbal; High level of accuracy and attention to detail; Exceptional computer skills with MS Office (Outlook, Word, Excel); Experience on LC-MS, Empower and Chromeleon software would be an asset Additional Information Accommodation: Eurofins welcomes all qualified applicants, including those with disabilities.

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 within commuting distance of North York, Ontario for showing an interest in this position.

Only those selected for an interview will be contacted.