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QAV Specialist

  1. Denmark
  1. Contract
Competitive
  1. CAPEX Projects
02-02-2024
33013

This vacancy has now expired

QAV Specialist – Life Sciences – Denmark – Contract

Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a QAV Specialist to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.

Responsibilities:
  • Create, approve and maintain quality plans and procedures.
  • Review and approve SAT/IQ/OQ and PQ for major process equipment being the isolator base filling line
  • QA involvement in clean room area readiness and qualification
  • Involvement in internal Mock-up audits to prepare for GMP inspection. 
Requirements:
  • Minimum 5 years QAV Biotech experience on Large Scale Projects
  • SME on all Quality and Compliance issues - minimum 5 years
  • Working knowledge of ASTM E2500 / Leveraging Verification process
  • Experience with design and construction projects for manufacturing facilities.
  • Experience with complex projects and working in or around operating facilities.
  • Ability to keep work pace and meet deadlines.
  • Good organising and planning skills.
If this role is of interest, please apply now.
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