Chemist, Quality Control Specialist

2 months ago

Richmond Hill, Ontario, Canada Apotex Full time
About Apotex Inc.

Apotex Inc. is a leading global pharmaceutical company that specializes in the development, manufacturing, and distribution of high-quality, affordable medicines for patients worldwide. With a strong presence in over 75 countries, Apotex employs a diverse team of professionals in various fields, including research and development, manufacturing, and commercial operations.

Job Summary

This role is responsible for generating accurate results while adhering to current Good Manufacturing Practices (cGMP) and regulatory requirements. The successful candidate will analyze various samples, including packaging materials, raw materials, and process validation samples, using a range of chemical and instrumental techniques.

Key Responsibilities
  1. Perform analysis of various samples using analytical instruments and established procedures.
  2. Compile and maintain accurate records of all analysis performed, including data and report summaries.
  3. Identify and report any out-of-specification or questionable results to the supervisor immediately.
  4. Assist in the completion of laboratory investigations under the direction of the supervisor.
  5. Perform daily calibration of laboratory equipment, such as balances and pH meters, in accordance with established procedures.
  6. Work collaboratively with the team to meet departmental goals and initiatives, sharing knowledge and expertise.
  7. Maintain compliance with all health and safety standards, regulatory requirements, and Apotex's policies and procedures.
  8. Provide technical support and training to team members as needed.
  9. Dispose of waste solvents and order laboratory supplies as required.
  10. Perform other relevant duties as assigned.
Requirements
  1. Education: Bachelor of Science in Chemistry or a related field from a recognized institution.
  2. Knowledge, Skills, and Abilities:
    1. Good theoretical understanding of FT-IR, titration, UV, and chromatography techniques.
    2. Excellent verbal and written communication skills.
    3. Knowledge of cGMP and problem-solving ability.
    4. Strong organization and time management skills.
  3. Technology/Instrumentation:
    1. UV, FT-IR, Karl Fischer Water Tester, pH meter, TOC analyzer, HPLC, UV, Dissolution, Titration, Fluorimetric, Column Chromatography, Auto-Titrator, Viscometer, TLC, Melting Point, Osmolality, Particulate Matter, Density, Seal Integrity, Particle Size Laser.
  4. Experience:
    1. Minimum of 1 year of relevant experience in the analysis of pharmaceutical products.

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