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QA Specialiste

September 24 2019
Industries Pharmaceutical, Biotechnology
Categories Production, Operations, Quality, Safety, Pharma, Biotech, Sciences, R&D, Chemistry, Quality, Test, Inspection, Scientific and Regulatory affairs, Quality assurance and control, Validation, Chemistry, Laboratory
Laval, QC

MS Pharma is looking for a specialist in Quality assurance.

At least three years of experience.

  • Complete knowledge of cGMP, GLP, BPD
  • Management of all controlled documents
  • Initiate investigations of Non compliance, CAPA, deviations and change control
  • Follow-up on corrective actions and quality systems
  • Verify and approve Certificates of Analysis
  • Manage internal audits and client audits
  • Follow-up on the efficacity of tranings of employees

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