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Downstream CQV Engineer

  1. Denmark
Copenhagen
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
09-05-2023
30986

This vacancy has now expired

Downstream CQV Engineer – Pharmaceuticals – Contract – Denmark

Reporting into the CQV Manager, this Downstream CQV Engineer will be responsible for the delivery of the Downstream CQV activities on a complex Biopharmaceutical manufacturing expansion project.

Downstream CQV Engineer Responsibilities:
  • Ensure Commissioning readiness of all Systems to support Process Equipment Start-up and IOQ Testing.
  • Lead execution of all CQV deliverables; IOQ, field execution.
  • Act as CQV SME on Process equipment
  • Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all Systems
  • 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 approve design reviews and protocols
  • Generate and ensure timely approval of all Commissioning and IOQ Final Reports
About you:
  • 4 years’ experience including experience with design and 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.
  • Strong communication skills.
  • Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)
Are you a good fit for this Downstream CQV Engineer position? We want to hear from you! Apply now.

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

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