Qa Systems Specialist
Pubblicato il 18-10-2026 - Gr?nenthal in Bardi
Select how often (in days) to receive an alert:Faccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura.Department: Global Operations & ProductionJob ID: *****Pay Range (tempo pieno): EUR 37.
Professional | Permanent | Full-time | On-SiteManufacturing & 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 likeEach day you'll enjoy a variety of challenges, such as:Coordinating Change Control processes, ensuring timely assessment, implementation and effectiveness verificationSupporting the development and execution of site training plans to ensure compliance with GMP and quality requirementsCoordinating the preparation, review and approval of Product Quality Reviews (PQRs), identifying trends and improvement opportunitiesPlanning and leading self-inspections, facilitating CAPA definition, implementation and effectiveness monitoringProviding QA oversight for the review and approval of Master Batch Records and associated GMP documentationLeading the preparation and review of process validation protocols and reports in collaboration with cross-functional teamsFacilitating risk assessment activities and promoting quality risk management principles across site operationsProviding strategic QA support for qualification and validation lifecycle activitiesOverseeing Quality Agreements with customers and external partners,
ensuring alignment with regulatory and business requirementsSupporting regulatory compliance activities and maintaining readiness for inspections and manufacturing license requirementsMonitoring and trending site Quality KPIs, identifying areas for improvement and driving related action plansActing as a key QA interface with internal stakeholders, promoting a culture of quality, compliance and continuous improvementWhat you'll bring to the tableTo make the most of this role and truly thrive, you should have:Degree in Scientific disciplinesMinimum 3 years of experience in Quality Assurance positions within the pharmaceutical sectorKnowledge of the local and international legal/regulatory requirements and GMP standardsCompetency in communication and interfaces managementOur 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.
xysqume In ****, Grünenthal employed around 4,300 people and achieved sales of € 1.8 billion.
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