Filter results by:
Sort by: relevance - date
You refined by: Montréal, QC (undo) JUBILANT DRAXIMAGE INC. (undo) undo all
Language
Upload your resume - Let employers find you

Quality Care Group of Companies jobs

Page 1 of 8 jobs
  • Perform all related tasks assigned by the Supervisor, Quality Control.
  • 3 years of experience in a microbiology laboratory, in a pharmaceutical quality control…
  • From the root cause analysis, write detailed Preventive Actions to minimize future similar quality events.
  • A culture that values opportunity for professional…
  • Assemble and lead the cross-functional product introduction and transfer team (R&D, Supply Chain, Manufacturing, Quality, Engineering, etc.).
  • Basic knowledge of Regulatory Affairs, Quality and Compliance, Quality Control and supply Chain tasks and responsibilities.
  • En français et en anglais).
  • Perform all related tasks assigned by the Supervisor, Quality Control.
  • 3 years of experience in a microbiology laboratory, in a pharmaceutical quality control…
  • From the root cause analysis, write detailed Preventive Actions to minimize future similar quality events.
  • A culture that values opportunity for professional…
  • Participates in External Audit activities / Quality Agreements, as needed.
  • Responsible in the maintenance of the Annual Product Quality System.
  • Quality audits and documentation in sterile would be an asset.
  • A culture that values opportunity for professional growth and development,highly competitive base…
  • Basic knowledge of Regulatory Affairs, Quality and Compliance, Quality Control and supply Chain tasks and responsibilities.
  • En français et en anglais).
  • Assemble and lead the cross-functional product introduction and transfer team (R&D, Supply Chain, Manufacturing, Quality, Engineering, etc.).
  • ISO 13485 Quality System management experience.
  • 21 CFR - Parts 820 Quality System Regulation.
  • A culture that values opportunity for professional growth and…
  • Prior knowledge and experience of the following standards:ISO 13485 Quality System management experience21 CFR - Parts 820 Quality System RegulationISO 14971…
  • Quality audits and documentation in sterile would be an asset.
  • A culture that values opportunity for professional growth and development,highly competitive base…
  • Participates in External Audit activities / Quality Agreements, as needed.
  • Responsible in the maintenance of the Annual Product Quality System.
  • ISO 13485 Quality System management experience.
  • 21 CFR - Parts 820 Quality System Regulation.
  • A culture that values opportunity for professional growth and…
» Post your resume - It only takes a few seconds