Found Description
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas .
We are currently seeking a skilled Technical CSV/CnQ Specialists with experience in the Life Sciences industry to support validation and qualification documentation activities within a long-term project.
The candidate will be responsible for the authoring, review, and lifecycle management of validation and qualification documentation, ensuring compliance with GxP requirements and industry standards.
This position is part of a long-term project based in the Canton Bern (Switzerland) and requires 100% on-site presence.
Responsibilities
- Preparation and maintenance of validation and qualification docum...
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