07 set - Varese
Gr?nenthal
Department: Global Operations & Production
Job ID: 45317
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
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
~ 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 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 premio.
Grünenthal offers equal employment opportunitie
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