Quality Assurance Specialist

Grünenthal Group; Origgio; Ibrido; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading company in pharmaceutical manufacturing is seeking a Quality Assurance Specialist in Origgio, Lombardy. The role offers a dynamic work environment where you will manage quality assurance processes and ensure compliance with GMP standards. Ideal candidates will possess a degree in scientific disciplines and have approximately two years of relevant experience. Join us to make an impact on product quality and regulatory compliance.

Competenze

• Previous experience in Quality Assurance (around 2 years).
• Knowledge of local and international regulatory requirements.

Mansioni

• Management of change controls and site trainings.
• Issuance and revision of Product Quality Review (PQR).
• Participation in self-inspections and CAPA management.

Conoscenze

GMP standards

Change control

Risk assessment management

Process validation

Fluency in English

Formazione

Degree in Scientific disciplines

Descrizione del lavoro

Join to apply for the Quality Assurance Specialist role at Grünenthal Group

Join to apply for the Quality Assurance Specialist role at Grünenthal Group

Professional | Permanent | Full-time | Hybrid

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 :

• Being part of the Quality Assurance team, reporting into the Head of QA Systems
• 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 and 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 :

• Previous experience in a similar role within Quality Assurance departments (around 2 years)
• Comprehensive knowledge of GMP standards and a previous experience in change control, risk assessment management and process validation, basic knowledge of the local and international legal / regulatory requirements
• Degree in Scientific disciplines
• Fluency in English

Seniority level

• Seniority levelEntry level

Employment type

• Employment typeFull-time

Job function

• Job functionQuality Assurance, Purchasing, and Manufacturing
• IndustriesPharmaceutical Manufacturing, Hospitals and Health Care, and Biotechnology Research

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Quality Assurance Specialist • Lombardia, Origgio, Italia