Associate Specialist QA Operations
Updated: May 28, 2024 02:10 PM GMT
STA Pharmaceutical Switzerland SA
Val-de-TraversAssociate Specialist QA Operations
Overview
QA Operations Team is committed to actively support the Couvet site and other departments to ensure cGMP compliant processes and products.
This position is responsible for quality assurance (QA) involved primarily with the review of bulk or packaged commercial drug products, raw material batches if required and maintaining working relationships with QA departments at contract facilities. The position will support on the floor QA activities (deviation, CAPA, OOS, change control, batch release, archiving, complaints ...) Couvet site included work in 2*8 shift if required. As a member of Quality Operations team, this position will be expected to be reliable source of information and interpretation of quality and cGMP compliance requirements. Furthermore, the position holder is responsible to identify and handle packaging, warehouse, or bulk/QC and cGMP compliance related issues. Additional tasks are quality metrics, risk assessments, as well... More Detail
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