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Sr QA Specialist - Biotech (GMP)

  • Standort:

    Amsterdam, Niederlande

  • Kontakt:

    Maaike Wagenaar

  • Jobtyp:

    Permanent

  • Kontakt Telefon:

    +31 (0)20 406 97 50

  • Branche:

    Pharmaceutical , Biotechnology

  • Kontakt-E-Mail:

    maaike_wagenaar@oxfordcorp.com

We are looking for a highly experienced QA-Officer for a biotech firm in Amsterdam. You oversee and coordinate a lot of different processes and handle non-routine QA-tasks.

Job Description

As Senior QA Specialist, you coordinate a few different systems, such as the internal audit program and the supplier qualification program. You handle non-routine tasks such as complex investigations and the implementation of corrective actions. You host external audits, perform internal audits, take on client questions, and so much more. You act as a point of seniority for the QA-team and you can simultaneously rely on management yourself for support. Overall, you have a varied and expert-level role in this quality assurance team. Feel free to reach out to our Science Recruiters with any questions, or apply if this sounds appealing!

Responsibilities

  • Coordinate the audit program
  • Handle deviations and change controls
  • Implement improvements
  • Perform internal audits
  • Host and support external audits
  • Stay up to date with GMP-guidelines and regulatory guidelines


Profile

  • Master's degree in a relevant field
  • At least 5 years of QA-experience in a GMP environment
  • Professional fluency in English is a required
  • Unlimited EU working permit is required.


Benefits

  • Long term position, direct contract with our client
  • Salary indication: €5000- €6500 gross monthly
  • Working hours: Full time, 32 hours up for discussion
  • Location: Amsterdam, on-site presence required, some remote work is possible
  • Vacaturenummer: 24852


IMPORTANT NOTE: Please do not apply if you do not have a working permit to live and work in the Netherlands. Your application will not be processed.