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Apotex

Analytical QC Chemist

18h

Apotex

CA · Full-time · C$60,000 – C$80,000

About this role

Apotex Inc. is a Canadian-based global health company producing high-quality, affordable generic, biosimilar, and specialty medicines accessible in over 75 countries. The Analytical QC Chemist carries out quality control, stability, method transfer, validation, and standard studies according to Standard Operating Procedures. This role supports manufacturing and R&D operations for nearly 7,200 employees worldwide.

Daily tasks involve testing raw materials, intermediates, finished products, R&D samples, and environmental samples using physical and chemical methods outlined in test methods, SOPs, compendia, and Certificates of Analysis. Perform sampling, inspection, labelling, and physical testing of packaging components while making routine decisions on simple priorities. Report deviations and maintain proper documentation of all analytical data.

Work collaboratively in a laboratory environment, liaising with higher-level personnel to learn equipment use and departmental practices. Keep the workplace clean, tidy, and safe, while reporting instrument or method issues promptly. Adhere to safety, quality, and compliance programs across the organization.

Demonstrate personal leadership through commitment to ongoing professional development and continuous learning. Seek performance feedback from peers, seniors, and supervisors to address gaps. Exhibit organizational values of Collaboration, Courage, Perseverance, and Passion.

Requirements

  • Minimum B.Sc. in Chemistry or equivalent area of study
  • Basic understanding of test methods, SOPs, compendia, and Certificates of Analysis
  • Basic analytical knowledge and experience for investigation activities
  • Ability to perform physical testing of packaging components and chemical testing of samples
  • Familiarity with laboratory equipment operation and calibration
  • Understanding of quality control testing procedures and documentation
  • Knowledge of GMP, stability studies, and method validation practices
  • Ability to follow SOPs strictly and seek guidance for non-routine matters

Responsibilities

  • Carry out quality control, stability, method transfer, validation, and standard studies according to Standard Operating Procedures
  • Perform labelling, inspection, sampling, and testing of raw materials, intermediates, finished products, and other samples
  • Conduct physical and chemical testing per test methods, SOPs, compendia, and Certificates of Analysis
  • Report all testing results, deviations, and problems with instruments or methods to Supervisor/Manager
  • Document analytical data accurately, self-review for completeness, and maintain records of retain, stability, and standard samples
  • Perform calibration of laboratory equipment according to the department’s calibration program
  • Liaise with laboratory personnel to learn physical and chemical testing equipment and regulatory practices
  • Keep the workplace clean, tidy, and safe while identifying needs for chemicals, gases, standards, and glassware