Analyst II R&D - BioPharma Product Testing Inc.

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. 900 laboratories in 61 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.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins Bio Pharma Product Testing Toronto, Inc. is seeking a detail-oriented and analytical Analyst II R&D to join our Research and Development team in Toronto, Canada. In this role, you will support the development and validation of analytical methods for pharmaceutical products, ensuring quality, safety, and regulatory compliance. You will work collaboratively with cross-functional teams to conduct testing, analyze data, and contribute to the advancement of our product portfolio.

• Develop, validate, verify, and transfer analytical methods for assay and impurities testing in accordance with ICH and regulatory guidelines.
• Perform routine and validation analysis using advanced analytical instrumentation including HPLC, GC, LC-MS/MS, and GC-MS/MS.
• Conduct analytical testing and quality control procedures on pharmaceutical products using appropriate laboratory techniques.
• Analyze and interpret complex analytical data, ensuring accuracy, completeness, and compliance with documentation standards.
• Prepare and review method validation/verification/transfer protocols and final reports with precision and clarity.
• Troubleshoot analytical methods and resolve technical issues to ensure consistent and reliable results.
• Support and conduct OOS/OOT investigations and assist in identifying root causes and corrective actions.
• Coordinate method transfer studies between clients and internal departments to ensure successful implementation and reproducibility of methods.
• Maintain accurate and organized laboratory records, ensuring full traceability and compliance with regulatory requirements.
• Review technical documents, data packages, and proposals as required.
• Collaborate with R&D scientists, Quality Assurance, and project managers to support product development initiatives.
• Assist with SOP training for new personnel and support SOP revisions as needed.
• Liaise with clients to maintain strong professional relationships and provide technical support.
• Provide ongoing technical guidance and training to staff to strengthen departmental capabilities.
• Stay current with emerging technologies, industry best practices, and regulatory updates relevant to pharmaceutical testing.
• Support the R&D Manager in departmental operations to ensure smooth workflow and achievement of business goals.

• Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline
• 5‑10 years of hands‑on experience in pharmaceutical R&D, product testing, or analytical laboratory environments
• Strong proficiency in analytical techniques and familiarity with laboratory instrumentation (HPLC, GC, mass spectrometry, or similar)
• Solid understanding of pharmaceutical quality control procedures and regulatory compliance standards (GMP/GLP)
• Excellent…