Expires soon SANOFI AVENTIS GROUPE

QUALITY COORDINATOR

  • V.I.E.
  • Geneva (Genève)
  • Master, Bac +5
  • Design / Civil engineering / Industrial engineering

Job description

Entreprise:
Program SaVIE (VIE of Sanofi) is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference on patients’ daily life, wherever they live and enable them to enjoy a healthier life.
Mission:
Due to increase of the complexity of the business (number of subcontractants) and of the legal and Sanofi requirements, we need support for the management of a part of the product/sub-contractant portfolio. This includes but is not limited to the management of QA (Quality Assurance), PQRs (Product Quality Review), releases preparation, audit and CAPA (Corrective and Preventive Action) follow up, risk management and complaints follow up for a product portfolio.
In addition, in order to efficiently close audit findings following the last GxP (Quality good practices) audit in Switzerland, the VIE will be involved in quality system activities which includes set up or revision of processes and creation of associated SOP (Standard Operating Procedures) and trainings in accordance with Sanofi global documents.
For a product portfolio:
- Quality Agreements management
- Risk Management
- Product Quality Review follow up
- Audit and CAPA follow up
- Market batch release preparation
- Complaints management
Additional Quality System activities:
- Sanofi Global Documents review and implementation on GMP/GDP (Good Manufacturing practices / Good Documentation Practices) related topics
- Setting or review of process and writting associated SOP and ensure appropriate trainings
The VIE will be responsible of a product portfolio and will be the business partner of a dedicated business unit.
Profile:
Education: Pharmacist or equivalent
Experience: previous experience in a pharmaceutical environment with knowledge of EU GMP and GDP is a plus
Professional skills / attitude and behaviour requested:
Organized
Fast learner
Ability with and interest on IT tools
Ability to work under stress and time pressure
FULL PROFICIENCY IN BOTH ENGLISH AND FRENCH IS MANDATORY
BASIC IN GERMAN IS MANDATORY

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