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Quality Control Inspector (Evening shift)

April 1 2020
Categories Production, Operations, Quality, Safety, Pharma, Biotech, Sciences, R&D, 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.

Requirements:

  • Minimum DEC in Science, or any related field;
  • B.Sc. in Science an asset;
  • DESS in QA/QC degree an asset;
  •  +2 years' experience in pharmaceutical;
  •  Experience in QA and/or QC a definite asset;
  •  cGMPs Regulations.

Other Criteria: 

  • Bilingualism, oral and written. Knowledge of Microsoft Office Tools. Great communication skills. Can multitask.
  • Result oriented. Cares about work well done. Time management. Teamwork. Meticulous. Attendance and punctuality.

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