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Department: Global Operations & Production

Job ID: 45317

Pay Range (tempo pieno) : EUR 37.

Professional|Permanent|Full-time|On-Site

Our people in

Manufacturing & Global Operations

share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain – from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future.

What the job looks like
Each day you'll enjoy a variety of challenges, such as:

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

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

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 interfac

📌 Senior QA Systems Specialist (Origgio)
🏢 Gr?nenthal
📍 Origgio