GMP Compliance Specialist

4 days ago


Copenhagen, Copenhagen, Denmark Optimus Life Sciences Full time
Key Responsibilities

In this role, you will be responsible for:

  • CQV activities: Carrying out hands-on CQV activities post-documentation phase, commissioning of process equipment, and ensuring GMP compliance.
  • Process commissioning: Executing the commissioning of various process & utilities including upstream and downstream processes/utilities and clean and black utilities.
  • Quality assurance: Maintaining GMP compliance for the engineering department and planning and supporting the qualification work for process plants and process equipment in the production areas.


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