Process Engineer

Vor 3 Tagen


Solothurn, Schweiz Michael Page Vollzeit

The selected candidate will be responsible for the following task area:

  • Designs, specifies, and installs new equipment for cell culture, purification, and pharmaceutical processes.
  • Provides engineering technical support, troubleshooting, and maintenance for production control systems and utilities.
  • Develops and oversees CQV (Commissioning, Qualification, and Validation) protocols, including testing and final report drafting.
  • Leads corrective and preventive actions (CAPA) and manages change controls for equipment and systems.
  • Acts as a subject matter expert in technical investigations and technology transfer for new processes and products.
  • Drives continuous improvement initiatives and optimizes equipment and facility performance.
  • Supports or leads project engineering efforts for new equipment installations and modifications.

To be considered for this position, the ideal candidate must have:

  • Successfully academic degree, ideally in (mechanical) engineering
  • At least 2 years of working experience in validation upstream and downstream processes
  • Proven experience in a GMP-regulated environment, including expertise in validation processes.
  • Excellent command of English (both written and oral), German would be an advantage
  • Proficiency with Delta-V, PLM, TrackWise, and CMMS (Infor) is a strong advantage.
  • Proven ability to address technical challenges and drive sustainable solutions.
  • Hands-on expertise in equipment lifecycle management and production systems.

Excellent project to join a well-known and prestigious pharmaceutical company with extension option.


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