Hybrid Commercial QA Specialist (m/f/d), 1-year contract (Paris la Défense, France) chez Grünenthal

​Professional  |  Temporary  |  Full-/ Part-time  |  Mobile Work​

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:

• Receiving Product Quality Complaints, collect information from complainants, analyze the investigation report, idenfiying if further actions (notification to Health Authorities, Recall, etc.) must be initiated
• Recording and investigating Deviations and Events
• Participate in preparation for GDP Audits and Inspections, monitoring applications of the Audits plans 
• Ensure timely and thorough execution of CAPAs to address identified quality issues 
• Redacting SOPs, support other departements if they need to review their SOPs,
• Management of Change controls impacting Gallia, and/or the French affiliate
• Following the KPIs, and monitoring, identification of trends
• Revue des APR/PQR for all the portfolio of distributed products
• Support the GDP activities for the French affiliate, within the cluster Gallia (France, Belgium, Luxemburg, Netherlands) and in Global Commercial Quality Assurance
• Ensures GDP-Training for onboarded collaborators, and periodic training

What you’ll bring to the table 
To make the most of this role and truly thrive, you should have:

• 3-5 years experience minimum in GMPs/GDPs in pharmaceutical industry
• Completed Pharmacist qualification, Registered as a pharmacist in Section B of the national register. 
• Experience in improving GMP and GDP compliance
• Business fluency in English and French
• Very good knowledge in MS Office applications

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