LCMSMS Analyst: GMP-Driven Method Development

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

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.