Supplier Quality Assurance Officer - Consumables M/F
Join Virbac SA, the historical and industrial heart of the Group. Join a unique site where global R&D (Research and Development) innovation, the excellence of our drug production plants, and the power of our logistics serving animal health coexist.
Join our Industrial Quality Assurance department in Carros (06), as a Supplier Quality Assurance Officer - Consumables (M/F) on a CDI (Permanent Contract), you will play a key role within the Quality Department.
Your challenge: Secure the regulatory compliance and excellence of our global network of consumable and single-use system suppliers to guarantee the integrity of our manufacturing processes and our products!
Proposed Missions:
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Perform quality audits of consumable suppliers in accordance with the defined annual program. *
Draft and negotiate Quality contracts with our partners according to company standards and requirements. *
Establish precise risk analyses for your scope of activity based on current procedures. *
Drive the monitoring of key performance indicators (KPI) to measure the effectiveness of our qualification activities. *
Ensure the approval and rigorous monitoring of our supply chains within our ERP (Enterprise Resource Planning / Progiciel de gestion intégré). *
Actively participate in strategic project meetings by providing your Supplier Quality Assurance expertise. *
Guarantee the update and compliance of Quality documentation in connection with international pharmaceutical regulations.
Frequent travel is to be expected for the performance of physical audits directly at our suppliers' sites.
Profile sought:
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You possess a higher scientific education at a Bac+5 level (Engineering degree or university equivalent). *
You have solid experience of 3 to 5 years in Quality Assurance, preferably in a similar or operational position within the pharmaceutical industry. *
You must master Quality Assurance frameworks (ISO 9001 - International Organization for Standardization) as well as pharmaceutical industry regulations (BPF - Bonnes Pratiques de Fabrication and its Annex 1, BPD - Bonnes Pratiques de Distribution, ISO 14644, ISO 13485 and USP 665 / USP 1665 requirements - United States Pharmacopeia). *
You demonstrate a strong technical appetite for manufacturing process analysis and excellent mastery of common IT tools (Pack Office, Google Workspace). *
You are fully comfortable in English (reading, writing, speaking), allowing you to conduct international audits and write clear and impactful reports. *
You are recognized for your team spirit, your advanced sense of Quality Culture, your ability to synthesize information, your technical curiosity, and your great adaptability.
Remuneration and benefits:
Remuneration according to your profile
This position has a Cadre status
To this remuneration are added variable remuneration elements, other social benefits, and teleworking days (according to the company agreement in force)
For candidates from outside the region, we support you in your geographic mobility through a mobility pack which includes:
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Personalized assistance in searching for your new accommodation, *
Financial support, *
Full coverage of your moving expenses.
Why not you? Choose a human adventure! Enjoy a rewarding environment, designed to release your potential and promote your evolution through the richness of our professions. Your expertise deserves an environment that matches it: join your talent with ours and let's build the animal health of tomorrow together.
What if your next challenge started here? Apply!