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CQV Engineer

  1. Denmark
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
04-05-2023
31275

This vacancy has now expired

CQV Engineer – Life Sciences – Contract – Denmark

Our client, a global specialist in biopharmaceutical 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:
  • Liaise with CQV PM and Lead Scheduler
  • Schedule, create and manage systems, ensuring all correct predecessors and successors are in place.
  • Ensure commissioning readiness of all systems to support process equipment start-up and IOQ testing.
  • 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 generate and approve design reviews, test matrices, risk assessments, various protocols and more.
  • Lead the execution of all CQV deliverables.
  • Act as the CQV SME on process equipment.
  • Generate and ensure timely approval of all commissioning and IOQ final reports.
About you:
  • 2 years’ experience including experience with ideally construction projects for biopharmaceutical manufacturing facilities. 
  • Experience with complex projects and working in or around operating facilities.
  • Experience within Drug Substance process areas.
  • Demonstrated proficiency communicating and collaborating at a variety of levels with customers, local vendors, equipment suppliers and operations staff.
  • Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)
Are you a good fit for this CQV Engineer position? 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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