Responsible for supporting the quality management system on review and approval of validation and engineering documents, test protocols, CAPAs, deviations, change controls and any technical documentation where QA needs to approve before implementation and upon completion.
Immediate availability required
Global pharmaceutical organization
The Regulatory Affairs Manager, reporting directly to the Head Medical & Regulatory Affairs / QA, will be responsible for managing and implementing the activities required obtaining and maintaining regulatory clearance with the local Authorities for the set array of products.
Join a great Company and Business in the Canton of Solothurn
Join one of the key players in the Generics and Brands arena
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