QC Chemist – GMP Lab Analysis & Instrument Troubleshooting

APOTEX; Toronto; On-site; CAD 49,000 - 81,000; Full time

Benefits offered by this job

Accommodation for disabilities

Bonus programs

Comprehensive benefits

Pension plan

Learning and development opportunities

Job summary

Apotex is a Canadian-based global health company headquartered in Toronto. The role analyzes laboratory samples and ensures results meet GMP/GLP standards, with data review and instrument maintenance responsibilities.

The candidate will perform analyses using HPLC, AA, UV, GC, IR, and UV/Vis spectrometry, while documenting observations and complying with regulatory requirements. Strong English communication and teamwork are essential.

Qualifications

• BSc in Chemistry or related field with 1 year pharma lab experience, or diploma with 2 years pharma lab experience.
• Proficiency in Excel, Word and lab software is an asset.
• Strong knowledge of automated instrumentation (HPLC, AA, UV, GC, IR, UV/Vis).
• Excellent verbal and written English communication and interpersonal skills.
• Knowledge of GMP/GLP and good documentation practices.

Responsibilities

• Perform analysis of laboratory samples and generate accurate results per SOPs and GMP.
• Document observations and data per established procedures and regulatory requirements.
• Review data for mathematical/analytical accuracy and sign off as trained.
• Operate and maintain lab instruments; troubleshoot with supervision as needed.
• Dispose waste solvents and order chemicals or lab supplies as required.
• Collaborate safely with team to achieve goals and demonstrate company values.
• Support QC documentation review and adherence to compliance programs.

Skills

Attention to detail

English communication

Interpersonal skills

GMP/GLP knowledge

Education

B.Sc. in Chemistry

Community College diploma

Tools

Excel

Word

Laboratory software

Job description

Apotex is a Canadian-based global health company headquartered in Toronto. The role analyzes laboratory samples and ensures results meet GMP/GLP standards, with data review and instrument maintenance responsibilities.

The candidate will perform analyses using HPLC, AA, UV, GC, IR, and UV/Vis spectrometry, while documenting observations and complying with regulatory requirements. Strong English communication and teamwork are essential.