Your mission:
- Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation.
- Ensure compliance to cGMP as well as maintaining equipment and facilities.
- Maintain training to the required level and support other functions on site.
- Execute manufacturing related work as per procedures and policies.
Your background:
- 5+ years’ experience in pharmaceutical drug substance manufacturing roles.
- Conversational English language (B1 minimum).
- Exposure to Delta V or Syncade or similar automated systems.
- Experience in highly regulated industry.
- Detail-oriented with strong understanding of automated systems and process controls.
What's on offer:
- A 12-month contract at an internationally known biotechnology company.
- Opportunity to develop in the position and company.
- A competitive, Swiss, salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter. #J-18808-Ljbffr