In order to continue to successfully support our various clients, we are currently actively looking for Qualification / Validation Engineers:
About the job:
- Write and execute qualification protocols; IQ, OQ, PQ
- Write equipment risk assessments (critical component assessments), Validation Plans, Requirement Tractability Matrix and qualification reports
- Co-ordinate qualification execution activities, including external vendors, internal departments, organizing materials, etc.
- Manage associated qualification deviations & CAPAs, including opening, resolution (with Supplier) and closure
- Participate in the creation and review of process Risk Assessments
- You hold a Master's in scientific or engineering discipline
- You have at least 3 years of experience in equipment qualification (IQ, OQ, PQ)
- You evolved in the Pharmaceutical and / or Biotech, or equivalent
- You are competent with current FDA and EU regulations and best practices
- You are fluent in English. Fluent in French and / or German is a big plus
- Human-sized company with colleagues from diverse cultural and professional backgrounds
- Open communication
- Joint team spirit
- Continuous learning and development thanks to internal trainings and workshops
At GXP Consulting Switzerland everyone contributes to our joint success and grows individually!
If you also share the same passion and values, we will be glad to hear from you!