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Job Summary

  • Switzerland
  • Contract
  • Ref ID: BBBH828158
  • Sep 13, 2022
  • Competitive

I am delighted to support a leading and reputable pharmaceutical company in their search for an experienced CQV engineer for a 12 month contract position.

Main responsibilities:

  • Preparation of documents associated with lifecycle of C&Q activities
  • Preparation of protocols
  • IQ / OQ
  • Preparation, execution and follow-up of Design Review (DR) and Design Qualification (DQ) protocol
  • Installation Verification execution
  • System Startup activities
  • Functional Testing of systems
  • Change Management activities during project lifecycle
  • Summary Report writing
  • Contractors and/or Vendors coordination

Skills & Experience

  • Minimum 3+ years experience in a CQV role.
  • Hands on expertise required within a pharma or med device environment
  • Experience with Regulatory and industry standards for GMP

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.

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