Design, program, test and commission industrial automation systems within highly regulated environments (GMP, GAMP 5, 21 CFR Part 11).
Your responsibilities :
* Programming, configuration and modification of industrial PLC systems → Siemens, Rockwell / Allen-Bradley (nice to have: Schneider, Beckhoff, Codesys)
* Development, implementation and maintenance of SCADA / HMI supervision systems → WinCC (TIA Portal), WinCC OA, FactoryTalk View, Ignition, or equivalent platforms
* Drafting and reviewing functional and technical documentation (URS, FDS, SDS, FAT/SAT/IQ/OQ protocols)
* Participation in FAT, SAT, commissioning and qualification phases (IQ/OQ/PQ)
* Providing Level 2/3 technical support to production and maintenance teams
* Ensuring strict compliance with GMP, GAMP 5, data integrity principles (ALCOA+) and OT cybersecurity requirements
* Monitoring technological developments in PLC, SCADA and IIoT solutions within the pharmaceutical industry
Your profile :
* Degree in Automation Engineering, Electrical Engineering or Industrial IT (HES/EPF or equivalent)
* 3–8 years of experience in PLC/SCADA programming within an industrial environment (pharmaceutical or biotechnology experience strongly preferred)
* Strong hands‑on expertise with Siemens or Rockwell automation platforms
* Solid experience with SCADA systems (WinCC, FactoryTalk View, Ignition or equivalent)
* Good understanding of GMP / GAMP 5 practices – a major asset
* Familiarity with equipment qualification and validation processes (FAT/SAT, IQ/OQ)
* Professional English (spoken and written); German is a plus
* Team-oriented, rigorous, autonomous, and comfortable working in multidisciplinary project environments
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