LCMSMS Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

Eurofins; Toronto; On-site; CAD 70,000 - 90,000; Full time

Job summary

A leading life sciences company in Toronto seeks an experienced LCMSMS Analyst responsible for method development, validation, and analysis in a cGMP lab. Candidates should have 3-5 years of experience in biopharmaceuticals and a strong background in Mass Spectrometry. This role requires relocation to Mississauga in 2026 and offers a chance to work in a dynamic laboratory setting with great career growth potential.

Qualifications

• 3-5 years experience in Pharmaceutical/Biopharmaceutical field in a GMP environment.
• Strong experience with Method Development, Validation, and Transfers.
• Solid background in Mass Spectrometry is mandatory.

Responsibilities

• Develop, validate, and analyze methods using LCMSMS.
• Prepare reports ensuring R&D projects meet timelines.
• Troubleshoot technical issues in the Analytical Laboratory.
• Perform instrument calibration and maintenance.

Skills

Method Development

Method Validation

Method Transfers

Computer proficiency - MS Office

Education

Bachelor of Science in Chemistry

Tools

LIMS

Empower

Analyst Software

HPLC-PDA

GCMSMS

Job description

LCMSMS Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

Full-time

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.

Under the direction of Department Head of R&D, LCMSMS analyst would be responsible for supporting the department analyzing Raw Material, Bulk & Finished Products in a cGMP laboratory that meets the departmental goal.

Key Responsibilities

• Perform Method Development, Method Validation, Method Transfer and Routine Analysis using LCMSMS and other instrumentation techniques.
• Reviewing data, preparing protocol and report to ensure R&D projects meet the timeline;
• Troubleshoot technical issues/ difficulties with all tests related with Analytical Laboratory;
• Perform instrument calibration, qualification and preventative maintenance program as necessary;
• Manage multiple research projects simultaneously to meet the project timeline;
• Verify that all study materials (including standards, reagents and columns) are in stock;
• Perform investigations and troubleshoot non-confirmatory results or methods;
• Understand and follow Quality System documents relevant to responsibilities, e.g. Quality Manual, SOPs, GMP/GLP/USP and Methods;
• Adhere to appropriate quality measures to meet or exceed the standards set by GMP government regulatory and company requirements relevant to assigned duties;
• Maintaining a neat and accurate record system of daily activities related with all R&D and Quality Control testing;
• Guide, mentor and train junior staff members to achieve expected quality and TAT metrics;
• Any tasks as required by supervisor or Management in all aspects of business to meet the departmental goals.

Qualifications

• A minimum of 3-5 years working experience in the Pharmaceutical/Biopharmaceutical field, in a GMP environment.
• Strong experience with Method Development, Method Validation, Method Transfers study.
• Computer proficiency-MS Office (Outlook, Word, Excel), LIMS, Empower & Analyst Software in a GMP environment.
• HPLC-PDA & GCMSMS experience would be an asset.

Education

• Bachelor of Science in Chemistry, or diploma in related field.
• A solid background of Mass Spectrometry is mandatory.

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

Working Conditions

This position will be working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses. Light lifting requirements of up to 20 kg.

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 atwww.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 atwww.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

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