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CQV Engineer

  1. Sweden
  1. Contract
  1. Commisions, Qualification and Validation
Date Posted13 Dec 2019

This vacancy has now expired

One of Quanta’s leading global pharmaceutical clients is looking for additional support within their CQV Team at their biologics fill-finish facility in Scandinavia.

Responsibilities will include:
  • Supporting the strategy for C&Q full lifecycle; testing; facility start-up; documentation and regulatory compliance
  • Carrying out the project C&Q master plan in line with the project objectives and goals. Ensure compliance to client and regulatory best practice
  • Interface with the other project teams to develop the overall C&Q phase project plan and schedule which includes risk assessment, design review/DQ, test matrix, FAT, SAT/commissioning, installation, operational and performance qualification for all systems
  • Completion of C&Q documentation development and management, and quality of the documentation library
  • Degree in Engineering or strong relevant experience
  • Extensive experience of working within a GMP environment
  • Previous experience of working within fill-finish facilities
  • Experience with current C&Q methods and industry best practice
  • Excellent problem solving and troubleshooting abilities
  • Ability to work in a fast-paced environment
 If this sounds like the role for you then please apply today!

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

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