Embedded in client site in Bern for PSS engagement
Focus on pathogen safety activities in viral safety
Support cross-functional stakeholders across TechOps, Reg Affairs, Manufacturing
Plan/execute pathogen safety risk assessments for changes
Prepare/ review pathogen safety docs and regulatory submissions
Contribute to virus validation and QbD-related activities

🎯 Requirements

Master’s or PhD in Life Sciences
3–5 years in R&D, Quality, or related pharma/biotech
GxP experience preferred; deviation/change assessments ideal
Strong virology/biochemistry/microbiology expertise
Fluent in English and German; cross-timezone collaboration
Academic-only backgrounds without industrial exposure not suitable

🎁 Benefits

Growth opportunities with learning and mentorship
Team-oriented culture with integrity and productivity
Equal opportunity employer statement

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