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CQV Engineer (Fill Finish)

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Onsite

CQV Engineer (Fill Finish)

EFOR

CQV Engineer (Fill Finish)

Skills

Testing & QACompliance

1 month ago

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Important information


Contract type:

Freelance / Contract

Location:

Munich, Germany

Work mode:

Onsite

Published on:

28 September 2026

What they need


About the Role:

We are seeking a skilled and motivated Process CQV Engineer to join our team for a high-profile pharmaceutical project in Munich. The successful candidate will be primarily responsible for the commissioning, qualification, and validation (CQV) of automated Optima filling lines. The role demands hands-on experience with pharmaceutical or biopharmaceutical filling lines, with a preference for Optima platform expertise.

Key Responsibilities:

  • Lead and execute CQV activities for automated Optima filling lines, including FAT/SAT, commissioning, IQ, OQ, and PQ protocols.
  • Develop, review, and approve CQV documentation in compliance with cGMP, FDA, and EU regulations.
  • Collaborate with project engineering, automation, quality assurance, and equipment vendors to ensure successful line start-up and handover.
  • Troubleshoot and resolve process and equipment issues during commissioning and qualification phases.
  • Support process characterization, cleaning validation, and media/batch simulation runs as required.
  • Drive continuous improvements and ensure efficient, high-quality CQV execution.
  • Maintain clear and concise project tracking, status updates, and reporting to management.
  • Adhere to all site standards relating to safety, quality, and documentation.

Requirements:

  • Bachelor’s degree (or higher) in Engineering, Pharmaceutical Sciences, or a related technical field.
  • Direct hands-on experience with automated pharmaceutical or biopharmaceutical filling lines is essential.
  • Specific experience with Optima filling lines strongly preferred; other major platforms (e.g., Bausch+Ströbel, IMA, Syntegon) also considered.
  • Proven track record in commissioning, qualification, and validation (CQV) of process equipment.
  • Excellent understanding of GMP, FDA, Annex 1, and other relevant regulatory guidelines.
  • Strong documentation skills and familiarity with risk-based qualification approaches.
  • Excellent troubleshooting and problem-solving abilities.
  • Effective communication skills in English; German language proficiency is advantageous.
  • Ability to work flexibly in a fast-paced, multi-disciplinary environment.

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