Experienced MES System Engineer for pharmaceutical manufacturing systems in GMP environment.
Support and optimize manufacturing execution systems in a regulated pharmaceutical or biotech facility, focusing on system maintenance, GxP compliance, and integration with automation and ERP platforms. Requires hands-on MES experience in life sciences, knowledge of batch records and validation, and understanding of IT/OT infrastructure. This is a one-year on-site contract in Switzerland with possible extension.
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Found at a specialist agency · listed 1 October 2026 · InsideJobs links you to the original posting.