HPLC Analyst - BioPharma Product Testing Inc.

HPLC Analyst I
- Eurofins Bio Pharma Product Testing Toronto, Inc.

• Full-time
• Compensation: CAD 45000 - CAD 55000 - yearly

Eurofins Scientific is an international network of independent life sciences companies, 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing.

It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 57 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.

The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades.

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.

A high level of professionalism and confidentiality is crucial to this role.

The Analyst must:

• Proficient in operating GC/HPLC/LC-MS/MS/GC-MS.
• 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.
• Recognizes OOS or out-of-trend results and assists laboratory manager in the completion of lab investigations.
• 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. Empower and Chromeleon, e-LIMS, ETQ etc.
• Troubleshoot technical issues/ difficulties with methods.
• Coordinate 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.
• Be experienced in a wide variety of routine and some non-routine wet chemistry methods and procedures.
• Strong interpretation of routine analysis or tests.
• In-depth understanding of chromatography principles, types and techniques.
• Have high troubleshooting skills, both with instruments and methods.
• Be able to write lab reports.
• Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods.
• 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.
• Competent research and study skills to learn about innovative methodologies and equipment used for…