Chemist, QC QS5

Apotex Inc.

. Perform analysis of laboratory samples including raw material, in-process, finished products, purified water, cleaning validation, stability samples, and analyses associated with method transfer or method verification .

Posted 10/26/2026contractNorth York • CanadaJunior💰 CA$48,851 - CA$81,419 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in laboratory analysis of pharmaceutical products, including proficiency with automated laboratory instrumentation and adherence to GMP/GLP standards. Strong organizational and communication skills support effective documentation and compliance with regulatory requirements.

Highest-signal resume keywords

Laboratory AnalysisAutomated Laboratory InstrumentationGMP/GLP KnowledgeProblem SolvingTime Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

HPLCAAUV SpectrophotometryDissolutionIRUV/VIS SpectrophotometryGCData AnalysisMathematical CalculationsDocumentation Practices

Soft Skills

Detail OrientedExcellent Communication SkillsOrganizational Skills

Tools & Technologies

Microsoft ExcelMicrosoft WordLaboratory Software Packages

Industry Keywords

Pharmaceutical Lab EnvironmentSOPsOOSOOTCompliance Programs

About the role

Key responsibilities & impact

Perform analysis of laboratory samples including raw material, in-process, finished products, purified water, cleaning validation, stability samples, and analyses associated with method transfer or method verification
Document observations and data from testing according to established SOPs and Good Documentation Practices
Recognize OOS, OOT, or anomalous results and assist with laboratory investigations under supervisor direction
Perform general maintenance and daily checks of laboratory equipment
Troubleshoot instrumentation and method problems with supervisor assistance
Dispose of waste solvents and order chemicals or laboratory supplies as required
Review and sign off completed electronic and/or paper data associated with trained analyses
Ensure results conform to specifications, GMP, in-house, compendial, and regulatory requirements; verify mathematical and analytical calculations
Adhere to organizational values and compliance programs, including business ethics, quality, safety, environmental, and HR policies
Perform other relevant duties as assigned

Requirements

What you’ll need

B.Sc. from a recognized educational institution in Chemistry or a related field and a minimum of 1-year relevant experience in a pharmaceutical lab environment; OR Community College diploma in a related field and a minimum of 2 years relevant experience in the analysis of pharmaceutical products
Knowledge of Excel, Work and other Microsoft Office Programs and/or laboratory software packages is an asset
Sound working and theoretical knowledge of automated laboratory instrumentation such as HPLC, AA, UV, Dissolution, IR, UV/VIS spectrophotometry and GC
Detailed oriented with problem solving and instrument troubleshooting ability
Excellent verbal and written English and communication skills
Knowledge of GMP/GLP
Proven organization and time management skills as demonstrated through previous work and/or educational experience

Benefits

Comp & perks

Bonus programs based on position in the organization
Pay-for-performance philosophy
Comprehensive benefits
Pension plan
Learning and development opportunities
Accommodation for applicants with disabilities during recruitment