Quality Control Supervisor

July 8 2024
Expected expiry date: August 6 2024
Industries Pharmaceutical, Biotechnology
Categories Quality assurance and control, Validation, Scientific and Regulatory affairs
Montreal, QC • Full time

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 25 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products. https://www.groupeparima.com

Quality Control Supervisor

The Quality Control Supervisor is responsible of the quality management of the QC Chemistry laboratory to ensure high standards and superior services while remaining compliant with regulations and safety programs. He/she ensures testing and release services (materials and products) are provided in support of established schedules.


  • Oversee and manage daily activities of the Quality Control team in an efficient manner
  • Oversee and coordinate raw material release internally and externally
  • Oversee and support internal and outsourced cGMP release and stability programs
  • Responsible of thorough completeness of deviations, Out of Trend (OOT) or Out of Specification (OOS) investigations.
  • Provide technical expertise and troubleshooting support, and ensure testing are completed in a timely manner
  • Responsible of all results released by the Quality control team
  • Lead and coach a team of QC Analysts
  • Perform mid-year and end of year evaluations
  • Assure the technical and safety trainings are kept updated
  • Support internal, client and regulatory agency audits as needed and develop action plans for continuous improvement
  • Serve as point person of all internal and external Quality Control data for commercial product
  • Ensure that instruments and equipment are kept in a qualified and calibrated state
  • Review periodical SOP revisions
  • Support the achievement of Groupe Parima global objectives

Skills and experience required

  • B.Sc. in Science (Chemistry, Biochemistry, pharmaceutical field) or related field f rom a Canadian University, or an equivalent scientific diploma recognized by a Canadian University or an accredited Canadian organism
  • Minimum of 10 years of experience in Quality Control in the pharmaceutical industry, with a minimum of 5 years in a management/supervisory position
  • Thorough knowledge and understanding of Canadian, US and European regulations
  • Experience with cGMP and ICH regulations and guidelines
  • Excellent interpersonal, organizational and communication skills
  • Bilingual (French and English)
  • Member of the Order od Chemists

What we offer:

  • Flexible work schedule and telework
  • Medical – dental & travel benefits
  • Group retirement plan
  • Recognition program & social activities
  • Personal days
  • Employee assistance program & online medical service
  • Hot Beverages (Hot chocolate, Coffee, Mokaccino)
  • Accessible by public transit or free parking
  • Referral program
  • Subsidized meal service
Apply now!

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