Pharmaceutical Commissioning Specialist

6 days ago


Copenhagen, Copenhagen, Denmark Optimus Life Sciences Full time
Job Description

We are seeking a skilled CQV Turnover Engineer to join our team at Optimus Life Sciences in Copenhagen, Denmark. As a mid-senior level professional, you will be responsible for carrying out hands-on CQV activities post-documentation phase, commissioning process & utilities, and ensuring GMP compliance.

Your responsibilities will include:

  • Commissioning of process equipment: Execute the commissioning of various process & utilities including upstream and downstream processes/utilities and clean and black utilities.
  • GMP compliance: 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.
  • Qualification and validation: IQ/OQ of Upstream and Downstream equipment/instrumentation, and ensure that all commissioning procedures are completed to ensure a smooth handover to operations is possible.


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