CQV Engineer – Copenhagen, Denmark – 12+ Month Contract

3 days ago


København, Denmark Optimus Life Sciences Full time

I am looking for an experienced CQV 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 Copenhagen, Denmark 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:

  • Perform practical CQV tasks following the documentation phase.
  • Carry out the commissioning of various process and utility systems, covering upstream and downstream processes/utilities, as well as clean and black utilities.
  • Take responsibility for organizing and coordinating all actions needed to maintain GMP compliance for the engineering department. Also, plan and assist in qualifying process equipment and process plants in production areas.
  • Conduct IQ/OQ testing on upstream and downstream equipment/instrumentation.
  • Ensure timely completion of assigned work within the project schedule, while adhering to engineering design standards and demonstrating equipment operability.
  • Assist other departments with the preparation and implementation of machine acceptance tests, and provide guidance for CQV activities at the site level.
  • Ultimately, ensure that all commissioning procedures are completed to facilitate a seamless handover to operations.

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

Engineering, Quality Assurance, and Project Management

Industries

Pharmaceutical Manufacturing and Biotechnology Research

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