QA Systems Specialist

Location: Origgio

Experteer Overview In Grünenthal’s Manufacturing & Global Operations, you help safeguard product quality across the value chain by leading change controls, PQR issuance, CAPA-driven improvements, and master data validation. You collaborate with cross‑functional teams to ensure regulatory compliance and licensing obligations are met while driving continuous quality improvements.

This role offers hands‑on QA responsibilities with meaningful impact on patient safety and product excellence.

Responsibilities Manage change controls across sites

Plan and execute site trainings

Issue and revise Product Quality Reviews (PQR)
Participate in self-inspections and CAPA management

Revise Master Batch Records Issue validation protocols and reports

Participate in risk assessment management

Cooperate in revising qualification and validation documentation

Oversee Quality Agreement with customers

Support regulatory activities to maintain manufacturing licenses

Collect and monitor site KPIs Qualifications Degree  in Scientific disciplines3–5 years of experience in Quality Assurance within pharmaceutical sector

Knowledge of local and international regulatory requirements and GMP standards

Competency in communication and interfaces management

Fluent English Benefits Performance -based annual bonus

Equal employment opportunities
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