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CQV Engineer

  1. Denmark
Copenhagen
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
30734

This vacancy has now expired

CQV Engineer – Pharmaceuticals – 12 Month Contract – Denmark

Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CQV Engineer 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.

CQV Engineer Responsibilities:
  • Oversee commissioning, Qualification and Validation of Drug Product facility systems which include multiple cold/freezer rooms and temperature-controlled units/rooms.
  • Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
  • Conduct FAT/SAT activities aligned to the current equipment vendor during installation and readiness.
  • Liaise with all project groups to ensure all Systems are managed appropriately for the Project Lifecycle.
  • Liaise with CQV Document Generation Lead in relation to generation and approval of relevant reviews, risk assessments and reports.
 About you:
  • 3 years’ experience including experience within the relevant equipment qualification.
  • Experience with complex projects.
  • Experience within generation of VPPs, risk assessments, and qualification protocols.
  • Previous experience of delivering FAT/SAT activities.
  • Ability to keep work pace and meet deadlines. Good organising and planning skills.
  • Proven success working well in a team environment with flexibility to react to changing business needs.
  • Computer skills (spreads, word processing, visio, Microsoft)
Are you a good fit for this CQV Engineer position? We want to hear from you! Get in touch with us today.

The candidate must have the rights to work in the location stated in the job advert.

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