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CQV Turnover Engineer – Copenhagen, Denmark – 12+ Month Contract

2 weeks ago


København, Denmark Optimus Life Sciences Full time

I am looking for an experienced CQV Turnover Engineer who is interested in working for one of the top-ranking companies in High-Tech Pharmaceutical Engineering. Join a team of hard-working Engineers in Ulm, Germany and gain valuable experience working on an exciting project in the biotech sector.

Positions Available: 1

Type: Contract (12+ months)

This role is available immediately, contact us now

Your Responsibilities:

  • Carry out hands on CQV activities post documentation phase
  • Execute commissioning of various process & utilities including upstream and downstream processes/utilities and clean and black utilities
  • Be responsible for planning and coordinating all measures to maintain GMP compliance for the engineering department as well as for planning and supporting the qualification work for process plants and process equipment in the production areas
  • IQ/OQ of Upstream and Downstream equipment/instrumentation
  • Ensure you complete your assigned work within the defined project schedule, ensure the engineering design standards are achieved and equipment operability demonstrated
  • Support and advise other departments in the preparation and implementation of machine acceptance tests
  • Eventually ensure all commissioning procedures are completed to ensure a smooth handover to operations is possible

Your Requirements:

  • You preferably have a university degree in pharmaceutical engineering, biotechnology or process engineering or a comparable subject
  • If you don’t have a degree, several years of professional experience in the field of commissioning/qualification/validation under GMP, are desirable with process systems and process equipment in production areas in the pharmaceutical or biotechnological environment
  • Experience working with upstream/downstream processes and equipment, clean and black utilities and HVAC
  • You are ready to work with different departments
  • You are independent and proactively prepared to do the hands-on activities
  • You are fluent in English

If you are interested in this role, please do not hesitate to send me your CV today for an immediate response

Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Industries: Pharmaceutical Manufacturing and Biotechnology Research
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