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Inspector, Quality Control

June 2 2021
Categories Production, Operations, Quality, Safety, Pharma, Biotech, Sciences, R&D, Quality, Test, Inspection, Quality assurance and control, Validation
Montreal, QC

Job Summary

  • Review batch records and release of manufacturing documents
  • Investigate discrepancies (e.g., non-conformities, Deviation)
  • Review In-process material records
  • Ensure manufacturing is followed in compliance with the Good Manufacturing Practices guidelines (cGMP's).

Responsibilities

  • Reviews production batch records and associated data for product release. Determines if records are within requirements of cGMP regulations. Reviews data obtained for compliance specifications and report and investigate abnormalities.
  • Inspect and release raw materials, packaging and printed materials for manufacturing.
  • Identify and report compliance issue and assist to resolve the issue.
  • Participate in investigation of complaints, deviations non-conformities and change controls.
  • Assure that all production personnel are complying with cGMP's.
  • Participate in self inspection program.
  • Perform other duties pertaining to QA and QC assigned by supervisor.
  • Act as a resource person for any quality issue.

Education: Minimum DEC in Science, or any related field; B.Sc. in Science an asset; DESS in QA/QC degree an asset

Experience: +2 years' experience in pharmaceutical; Experience in QA and/or QC a definite asset 

Technical Know-How: cGMPs Regulations; Good knowledge of Microsoft Office and Outlook programs

Other criteria: Bilingualism, oral and written; Knowledge of Microsoft Office Tools; Communication skills; Be able to multi-task; Result oriented; Cares about work well done; Time management; Teamwork; Meticulous in their work;

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