Medicine and Pharmaceuticals

Process Equipment C&Q Engineer

Mainz GermanyOn-siteFreelanceStart date 1/202612 + Months
Contact person
Greg King
Project ID
2948854
BioprocessGood Manufacturing PracticesEngineeringRecruitmentSession Initiation ProtocolsPharmaceuticalsQuality ManagementRisk AnalysisTest PlanningIq/oq/pq

Description

We are seeking a Commissioning & Qualification (C&Q) Engineer with strong experience in pharmaceutical process equipment. You will support equipment installation, commissioning, and GMP qualification activities across pharmaceutical and biotech manufacturing sites in Germany.
Key Responsibilities

  • Execute commissioning, IQ/OQ/PQ qualification for pharmaceutical process equipment (e.g., bioreactors, mixers, CIP/SIP systems, filtration systems, filling/packaging equipment).
  • Prepare and review C&Q documentation: protocols, test plans, reports, risk assessments.
  • Support FAT/SAT, equipment start-up, troubleshooting, and performance verification.
  • Ensure full compliance with EU GMP, Annex 15, GAMP 5, and internal quality standards.
  • Collaborate with engineering, QA, and suppliers to meet project deadlines and quality expectations.
Requirements

  • Degree in Engineering (Mechanical, Chemical, Bioprocess, or related).
  • Experience in pharma/biotech equipment C&Q is essential.
  • Strong understanding of GMP and validation principles.
  • Fluency in German (C1 or native); English preferred.
  • Ability to interpret P&IDs, URS/FS/DS, and equipment documentation.
  • Willingness to work onsite in Germany.


Darwin Recruitment is acting as an Employment Business in relation to this vacancy.

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