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Quality Assurance Coordinator

Employment Date display: 09/12/2025 #Ref.:7596

Salary :

Activity area : Industrial and manufacturing

Post category : Production and engineering

Province : Quebec

Region : Montreal

Recruiter : Francois Vedel

Contact us : fvedel@st-amour.com

Job description :

Our plant, which specializes in the manufacture of industrial chemicals, is looking for a Quality Assurance Coordinator to strengthen its quality system and support operations. You will play a central role in ensuring compliance with standards, regulations, and safety standards in a chemical environment.

Main responsibilities

  • Implement good manufacturing practices for regulated products and quality standards to maximize the manufacturing quality of operations;
  • Ensure the smooth operation of the laboratory;
  • Coordinate quality assurance systems in accordance with current regulations (Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP));
  • Coordinate the maintenance program for equipment related to the manufacture of regulated products;
  • Coordinate the stability program, including the approval of stability reports;
  • Coordinate customer complaints related to GMP;
  • Coordinate employee training;
  • Draft standard manufacturing and packaging formulas for regulated products;
  • Draft protocols and validation reports;
  • Manage documentation, including developing or updating procedures;
  • Manage change.
  • Manage CAPA events, including approving deviation and non-compliance reports (including Out of Specification reports).
  • Draft APQRs.
  • Coordinate internal audits.
  • Ensure the application of policies, GMP standards, and regulations across all departments under your responsibility.

Skills and qualifications :

  • DEC with experience or Bachelor's degree in chemistry or biochemistry or any other recognized training relevant to the position
  • Minimum of three (3) years of experience in manufacturing (pharmaceutical industry, chemicals);
  • Mastery of Good Manufacturing Practices (GMP),
  • Knowledge of continuous improvement methods (Kaisen, 5S, M, etc.) an asset;
  • Knowledge of labor and OHS standards and ISO 9001 standard an asset;
  • Knowledge of an integrated management system (ERP)
  • Fluency in spoken and written English essential;
  • Good command of MS Office suite.

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