HPLC Analyst I - Eurofins BioPharma Product Testing Toronto, Inc.

Eurofins · Toronto, ON, Canada

  • Senior
  • Full-time
  • Posted 2026-09-04
  • Confirmed live on 25 September 2026

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Job description

Job Description
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 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.
WORKING CONDITIONS:

• This position will be working in a laboratory environment where standing is required for greater than 50% of the time. Light lifting requirements of no more than 30 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE.

• Shift work and overtime may be required, as well as working

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