We are searching for a Senior Qualification & Validation Engineer for a 6 - 12 month project supporting a Global Pharmaceutical company HQ in Switzerland
Key Responsibilities:
Create Qualification Documents:
- Developing and creating qualification protocols (IQ, OQ, PQ) from scratch for equipment, facilities, and systems
- Generating documents such as URS, FAT/SAT, and traceability matrices
- Collaborating with teams to gather technical data for documentation
Experience needed:
- Experience with GMP requirements (Annex 11, data integrity, GAMP 5, etc.)
- Experience in the field of Qualification / Validation in highly regulated environments
- Fluent German and English is required for this role
If this opportunity is for you, apply using the link provided
*Please note, only those with a right to work in Switzerland can be considered (Visa sponsorship not provided)
