Associate Specialist QA Operations

Updated: June 13, 2024 04:12 AM GMT

STA Pharmaceutical Switzerland SA

Val-de-Travers

Associate 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