ph3Responsibilities /h3 ul liManagement of change controls /li liParticipation in planning and execution of site trainings /li liIssuance and revision of Product Quality Review (PQR) /li liParticipation in planning and execution of self‑inspections together with CAPA management /li liRevision of Master Batch Records /li liIssuance of process validation protocols and reports /li liParticipation in risk assessment management /li liCooperation in the revision of qualification and validation documentation /li liOverview on Quality Agreement with customers /li liParticipation in management of regulatory aspects to maintain required manufacturing licenses /li liCollection of site KPIs /li /ul bRequirements /b ul liDegree in Scientific disciplines /li li3–5 years of experience in Quality Assurance positions within the pharmaceutical sector /li liKnowledge of the local and international legal/regulatory requirements and GMP standards /li liCompetency in communication and interfaces management /li liFluent English /li /ul /p #J-18808-Ljbffr

📌 QA Systems Specialist (Origgio)
🏢 Jobtailor
📍 Origgio