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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