GC / GCMSMS Analyst II

LabRulez; Toronto; Hybrid; CAD 65,000 - 90,000; Full time

Benefits offered by this job

Health & dental benefits

RRSP with company match

Paid holidays & PTO

Job summary

Eurofins Scientific in Mississauga, Ontario, is seeking a GC/GCMSMS Analyst II to provide analytical support in the Biopharmaceutical Chemistry Testing Laboratory. The role emphasizes GC instrumentation, method development, validation, and GMP compliance.

You will work with customer-oriented teams, maintain data integrity in LIMS, and grow your expertise across HPLC, LC-MS/MS, ICP-MS and related software while ensuring safe and efficient laboratory operations.

Qualifications

• 2–7 years of experience with analytical instrumentation.
• Experience with GC, GC-MS/MS, GC-FID and GC detectors.
• Ability to work under GMP/GLP and SOPs.
• Strong documentation and data integrity skills.
• Willingness to relocate to Mississauga, ON in 2026.

Responsibilities

• Sample preparation and mobile phases preparation.
• Documentation: accurate reporting in lab books.
• Operate GC, HPLC/UPLC, UV, IR and other instruments for analysis.
• Mentor junior staff and assist with instrument maintenance.
• Ensure compliance with GMP/GLP and SOPs.

Skills

GC/GCMS

GCMSMS

Analytical instrumentation

Data integrity

LIMS experience

Education

B.Sc. in Chemistry or related field

Tools

Chromeleon

Mass Hunter

e-LIMS

eQMS

Excel

Job description

Analytical chemist, Gas chromatography, Gas chromatography-mass spectrometry

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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

GC/GCMSMS Analyst II

Job Description

Reporting directly to the Director - Chemistry, the Analyst II 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 II will have over 2 to 7 years of laboratory testing experience with demonstrated ability to complete role/duties that are more complex. Has handled variety of instrumentations 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 GCMS or GCMSMS and GC instruments with headspace FID and TCD detectors.
• Perform method development, method validation, method transfer and routine analyses using GC-MS/MS and GC-FID instrumentation.
• Learn and apply knowledge with additional advanced instrumentation techniques (HPLC, LC-MS/MS, ICP-MS, etc.) and software (Waters, Chromeleon, Analyst, Mass Hunter) as necessary
• Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
• Perform instrument calibration, qualification and preventative maintenance program as necessary.
• Analyze API, Raw Materials and Finished products for Assay, Impurities/ Residual solvents/ Pesticide analysis using GC instrument with minimum or no supervision.
• Recognizes OOS or out of trend results and assists laboratory manager in the completion of lab investigations.
• Calibrate instruments.
• Process and report analytical results.
• Update and report work into LIMS.
• 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. Chromeleon, Mass hunter, e-LIMS, eQMS etc.
• Troubleshoot technical issues/ difficulties with methods.
• Co-ordinate 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.
• 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.
• Apply technical judgment to determine potential problems for samples.
• Appropriately follow safety, operational integrity and quality control requirements for the work that is done.
• 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 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 trouble shoot instrumentation/methods
• Perform other departmental tasks such as cleaning, supply ordering, assist with instrumentation training and maintenance, etc
• Perform analytical tests utilizing GC, HPLC/UPLC, 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 GC/GCMS/ 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:

• 2-7 years working with analytical instrumentation.
• Ability to work directly from the USP or EP pharmacopeia 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 periodic weekends and/or evenings.

Additional Information

Please note that relocation to Mississauga, ON is expected in 2026.

Disclaimer:Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation:Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca .

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work.To learn more about Eurofins, please explore our website at www.eurofins.ca

This posting is supported by AI technology to assist in screening candidates and resumes.

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