LCMS/MS Analyst – R&D, GMP, Method Development

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

Job summary

A leading life sciences company in Toronto seeks a LCMSMS analyst to support the R&D department. The candidate will analyze raw materials and products in a cGMP lab, performing method development and validation, troubleshooting issues, and mentoring junior staff. Applicants should have 3-5 years experience in the Pharmaceutical/Biopharmaceutical field, a Bachelor’s in Chemistry, and a solid background in Mass Spectrometry. Full-time position, requires relocation to Mississauga in 2026.

Qualifications

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

Responsibilities

• Perform Method Development, Validation, Transfer and Routine Analysis using LCMSMS.
• Review data and prepare protocols and reports for R&D projects.
• Troubleshoot technical issues with all tests related to Analytical Laboratory.

Skills

Method Development

Method Validation

Computer proficiency-MS Office

LIMS

Empower

Analyst Software in a GMP environment

Troubleshooting technical issues

Education

Bachelor of Science in Chemistry

Diploma in related field

Tools

HPLC-PDA

GCMSMS

Job description

A leading life sciences company in Toronto seeks a LCMSMS analyst to support the R&D department. The candidate will analyze raw materials and products in a cGMP lab, performing method development and validation, troubleshooting issues, and mentoring junior staff. Applicants should have 3-5 years experience in the Pharmaceutical/Biopharmaceutical field, a Bachelor’s in Chemistry, and a solid background in Mass Spectrometry. Full-time position, requires relocation to Mississauga in 2026.