Director Quality Transformation & Site Excellence
Pubblicato il 19-10-2026 - Grünenthal Group in Bardi
pProfessional | Permanent | Full-time | Hybrid /p pOur people in bManufacturing Global Operations /b 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.
/p h3What The Job Looks Like /h3 pEach day, you'll enjoy a variety of challenges, such as: /p ul liLead quality assessments and diagnostics at manufacturing sites.
/li liProvide hands-on support to sites facing compliance, inspection, performance, or quality system challenges.
/li liServe as interim Quality leader or advisor during critical business situations, leadership transitions, or remediation programs.
/li liEnsure sustainable resolution of quality risks, deviations, audit findings, and systemic compliance gaps.
/li liLead regional quality transformation programs and strategic improvement projects.
/li liSupport post-merger integrations, site transfers, network harmonization initiatives, and quality culture transformations.
/li liCoach and develop site Quality leaders and quality teams.
/li liStrengthen quality culture and continuous improvement capabilities at site leadership level.
/li /ul h3What You'll Bring To The Table /h3 pTo make the most of this role and truly thrive, you should have: /p ul liMaster's Degree in Pharmacy, Chemistry, Biology, Biotechnology, Engineering or related Life Sciences discipline.
/li li15+ years of experience within pharmaceutical Quality functions.
/li liSignificant experience as: Site Head of Quality/ Head of QA/ Senior Quality Leader within GMP-regulated environments.
/li liDemonstrated experience supporting FDA, EMA and international regulatory inspections.
/li liProven track record managing complex remediation programs and quality transformations.
/li liExperience leading cross-functional and multi-site initiatives within global pharmaceutical organizations.
/li liExperience participating in mergers, acquisitions, site integrations or large-scale organizational change programs is advantageous.
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