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Quality Assurance Specialist

June 12 2017
Industries Pharmaceutical, Biotechnology
Categories Medical and pharmaceutical information, Quality assurance and control - Validation, Scientific and Regulatory affairs
Laval, QC

MAIN TASKS:

  • Revision of batch records.

  • Monitoring of master documents.

  • Writing and monitoring of SOP.

  • Writing and revision of validation and stability protocols.

  • Monitoring of quality complaints, deviations, CAPA and change control systems.

  • Suppliers Audits.

  • Monitoring of retains and stability samples.

  • Evaluation of returns.

  • All other functions related to GMP compliance.

    REQUIREMENTS:

  • Bachelor degree in Science or in a related field.

  • Perfect knowledge of GMP.

  • Minimum of 5 years' experience in the pharmaceutical industry.

  • Perfectly bilingual (English & French).

  • Strong ability for solving complicated situation.

  • Ability to work under minimal supervision.

  • Ability to monitor multiple priorities and strong organizational skills.

  • Good knowledge of Microsoft Office (Word, Excel, PowerPoint, Access, etc.)

  • Excellent in written and verbal communications.

  • Car owner

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