Analyst (hplc) - Eurofins Biopharma Product Testing Toronto, Inc.

Analyst (HPLC) - Eurofins BioPharma Product Testing Toronto, Inc.

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 ongoing 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 II 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 problem-solving and troubleshooting.
• Accountable for the integrity and traceability of all data generated and reported.
• Design, preparation, and production of study materials including procedure manuals.
• Perform other duties as assigned by the Laboratory manager.

Key Responsibilities:

• Sample preparation and Mobile phases preparation.
• Documentation: Ensuring accurate reporting in lab books.
• Using a wide range of sophisticated equipment and instruments to conduct analysis and research and troubleshoot instrumentation/methods.
• Perform other departmental tasks such as cleaning, supply ordering, assist with instrumentation training and maintenance, etc.
• Perform analytical tests utilizing HPLC/UPLC, GC, UV, IR, FTIR, KF and other laboratory instruments.
• Assess, compare and perform risk assessments for compendial method compliance according to USP, EP, and other regulations.
• Mentoring/training junior staff members and Imparting training to new recruits for operation, calibration and preventive maintenance of GCMS/GC/HPLC/ LC-MS/MS, etc.
• Writing SOPs.
• Ensure that work is performed in compliance with good manufacturing practices (GMP), standard operating procedures (SOPs) and the current test method.
• Participates in general lab duties, including clean-up, administration, logbook review and operations support.

Qualifications

Education:

• A B.Sc. degree preferably in Chemistry, or diploma in related filed.
• A solid background and understanding of Chemistry is mandatory
• Computer proficiency- Microsoft Office, especially Excel

Experience:

• 5-10 years working with analytical instrumentation.
• Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods
• Experience working in contract Laboratory considered an asset.
• Experience working with Pharmaceuticals.

Please note that this role will require relocation to the Company's Mississauga office following our planned office move in 2026.