Chiesi Research & Development is recruiting for a Pharmacovigilance QA specialist to ensure the PV quality system complies with regulatory standards across the organization. You will manage deviations, CAPAs, and assist in inspections, with close collaboration to the QPPV and cross-functional teams.
The role requires a Life Sciences degree and 3–5 years in pharmacovigilance/QA, strong knowledge of PV regulations, and fluency in English.
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