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 c ommissioning, 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.