Junior QA Systems Specialist

Gr?nenthal GmbH; Origgio; In loco; EUR 34.000 - 35.000; Tempo pieno

Descrizione del lavoro

Grünenthal seeks a professional to join Global Operations & Production in our manufacturing operations team. This role is full-time and on-site, operating within an international, collaborative environment focused on quality and continuous improvement.

You will contribute to change controls, Product Quality Reviews, Master Batch Records, and validation documentation, while helping ensure quality agreements with customers and tracking site KPIs.

Competenze

• Degree in scientific disciplines.
• Strong communication and interfaces management skills.

Mansioni

• support in management of change controls
• issuance and revision of Product Quality Review (PQR)
• revision of Master Batch Records
• support in process validation protocols and reports
• cooperation in the revision of qualification and validation documentation
• overview on Quality Agreement with customers
• collection of site KPIs

Conoscenze

communication

interfaces management

Formazione

Degree in scientific disciplines

Descrizione del lavoro

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Department: Global Operations & Production

Job ID: 45451

Department: Global Operations & Production

Pay Range (full time): EUR 34.000 - 35.000

Professional | Temporary | Full-time | On-Site

Our people inManufacturing & Global Operationsshare 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:

• support in management of change controls
• issuance and revision of Product Quality Review (PQR)
• revision of Master Batch Records
• support in process validation protocols and reports
• cooperation in the revision of qualification and validation documentation
• overview on Quality Agreement with customers
• 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
• competency in communication and interfaces management

Our pay ranges are based on an objective, gender-neutral job evaluation system. The final salary offered is determined based on factors like, but not limited to, relevant education, skills, experience, certifications, geographic location, and business or organizational needs. Your compensation package will include a performance-based annual bonus.

Grünenthal offers equal employment opportunities. Recruitment will take place without distinction with regard to religion, gender, sexual orientation, age, origin, disability or other relevant categories.

Grünenthal is a global leader in pain management and related diseases. As a science-based, privately-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to patients worldwide. Our purpose is to change lives for the better – and innovation is our passion. We are focussing all of our activities and efforts on working towards our vision of a world free of pain.

Grünenthal is headquartered in Aachen, Germany, and has affiliates in 28 countries across Europe, Latin America and the US. Our products are available in more than 100 countries. In 2024, Grünenthal employed around 4,300 people and achieved sales of € 1.8 billion.