Responsibilities - Management of change controls - Participation in planning and execution of site trainings - Issuance and revision of Product Quality Review (PQR) - Participation in planning and execution of self‑inspections together with CAPA management - Revision of Master Batch Records - Issuance of process validation protocols and reports - Participation in risk assessment management - Cooperation in the revision of qualification and validation documentation - Overview on Quality Agreement with customers - Participation in management of regulatory aspects to maintain required manufacturing licenses - Collection of site KPIs Requirements - Degree in Scientific disciplines - 3–5 years of experience in Quality Assurance positions within the pharmaceutical sector - Knowledge of the local and international legal/regulatory requirements and GMP standards - Competency in communication and interfaces management - Fluent English
📌 QA Systems Specialist (Origgio)
🏢 Jobtailor
📍 Origgio
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