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GCMSMS Analyst II - Eurofins Biopharma Product Testing Inc.

Job in Toronto, Ontario, C6A, Canada
Listing for: Eurofins-Canada-Biopharma
Full Time position
Listed on 2026-07-14
Job specializations:
  • Pharmaceutical
    Analytical Chemist, Pharmaceutical Science/ Research, Medical Technologist & Lab Technician
Salary/Wage Range or Industry Benchmark: 55000 - 70000 CAD Yearly CAD 55000.00 70000.00 YEAR
Job Description & How to Apply Below
Position: GCMSMS ANALYST II - Eurofins BioPharma Product Testing Inc.

GCMSMS ANALYST II - Eurofins Bio Pharma Product Testing Toronto, Inc.

  • Full-time
  • Compensation: CAD 55,000 - CAD 70,000 yearly

Reporting directly to the Director of Chemistry, the Analyst II will provide technical support and analysis within the Biopharmaceutical Chemistry Testing Laboratory in a deadline-based, high-pressure environment with ongoing projects for multiple clients. The position requires 2 to 7 years of laboratory testing experience and will be based in the Company’s Mississauga office following relocation in 2026.

Responsibilities
  • Operate GCMS/GCMSMS and GC instruments with headspace FID and TCD detectors.
  • Develop, validate, transfer, and routinely analyze samples using GC-MS/MS and GC-FID instrumentation.
  • Apply advanced instrumentation techniques (HPLC, LC-MS/MS, ICP-MS) and supporting software (Waters, Chromeleon, Analyst, Mass Hunter).
  • Ensure compliance with Safety policies, GMP/GLP, and SOPs.
  • Perform instrument calibration, qualification, and preventative maintenance.
  • Analyze API, raw materials, and finished products for assay, impurities, residual solvents, and pesticide residues.
  • Identify out-of-specification or out-of-trend results and assist laboratory manager with investigations.
  • Process, report, and enter results into LIMS.
  • Review technical data, documents, and proposals.
  • Use Microsoft Office (Outlook, Word, Excel) and pharmaceutical data acquisition software.
  • Troubleshoot technical issues with methods and instruments.
  • Coordinate method transfers between R&D and QC groups.
  • Maintain safe and healthy laboratory environment.
  • Interpret routine analyses and apply chromatography principles.
  • Execute work under GMP guidelines and USP/pharmaceutical testing standards.
  • Document SOPs, study materials, and procedures.
  • Mentor and train junior staff on instrumentation and SOPs.
  • Perform other duties assigned by the Laboratory Manager.
Key Responsibilities
  • Prepare samples and mobile phases.
  • Ensure accurate reporting in lab books.
  • Operate a wide range of analytical instruments and troubleshoot as needed.
  • Conduct cleaning, supply ordering, and instrument training/maintenance activities.
  • Perform analytical tests using GC, HPLC/UPLC, UV, IR, FTIR, KF and other instruments.
  • Assess risk for compendial method compliance with USP, EP, and other regulations.
  • Write SOPs and ensure GMP compliance.
  • Participate in general lab duties and operations support.
Education
  • B.Sc. degree in Chemistry or related field.
  • Solid background in Chemistry.
  • Computer proficiency – Microsoft Office, especially Excel.
Experience
  • 2–7 years working with analytical instrumentation.
  • Ability to work directly from USP or EP pharmacopeia and execute methods.
  • Experience in contract laboratories is an asset.
  • Experience working with pharmaceuticals.
Working Conditions
  • Laboratory environment requiring >50% standing; light lifting ≤30 lbs.; hazardous materials handled with PPE.
  • Shift work and overtime, including periodic weekends and evenings.
  • Relocation to Mississauga, ON expected in mid‑2026.

Benefits include health and dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off, and additional comprehensive total rewards package which will be discussed during the interview.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

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