Responsibilities
- Contribution to the integration of new production equipment and utilities in a biotech/pharma environment
- Creation of specifications (URS) and risk analyses (FMEA, FRA)
- Creation and review of the Validation Master Plan (VMP)
- Participate in the creation and writing of test protocols for commissioning and qualification: FAT/SAT/IQ/OQ/PQ according to GMP requirements
- Participate in commissioning at suppliers (FAT)
- Participate in commissioning on customer site (SAT)
- Perform installation and operational tests (IQ/OQ/PQ)
- Work under the supervision of a Lead Validation
Requirements
- Engineering degree in biotechnology, pharmaceutical sciences, process engineering or industrial pharmacist (PharmD)
- Experience in process validation and equipment qualification in a GMP environment
- Understanding of biotechnology production processes (USP, DSP, F&F) essential
- Good Manufacturing Practices
- Fluent in German and English
Benefits
- Joining a group with strong development potential that aims to improve your employability on challenging and varied projects
- Joining a structure that has been established in Switzerland for a long time with a client portfolio that includes leaders in the sector
- Having a sustainable job with stability and access to a real collaboration
- Benefit from training with accredited and certified centers
- Having a local management team to support you in the achievement of your missions and in the development of your career
- Being part of a dynamic, committed team with real human values that we live by every day
Work Arrangement
Remote (Country) — Switzerland
Additional Information
- Only applications from Swiss and EU citizens will be considered
