Postes de Santé & Sciences de la Vie - Affaires règlementaires
7 offre(s) d’emploi correspondant(es)
- InternationalPermanentCHF74,818 - CHF96,195
For our client we are exclusively looking for a Senior Quality Manager in the area of South Holland. In this role you are responsible for providing direction and leadership of the quality department within the organization by focusing on quality control and quality assurance.
- Quality Assurance
- Medical Device Industry
For our client Sanofi Genzyme we are exclusively recruiting a new Project Manager & Associate Regulatory Affairs (RA). We are looking for candidates who have a strong analytical mind and an eye for detail. Are you result-driven, accurate and do you have good planning skills? Then we might be looking for you!
- Challenging combination of Regulatory Affairs and Project Management
- Working for a world leading biotechnology organisation
To cover temporary leave employment from 06 June 2017 to 18 August 2017.
- Regulatory Operations
- Submission Publishing
Michael Page is working on a Senior role and looking for a very hands on candidate that is keen to join a new adventure in an international company, being responsible for the Regulatory Affairs team in Europe. Flexibility to travel in (and outside) Europe is important.
- Senior and hands on role for a Senior Director Regulatory Affairs
- Experience and proven trackrecord in the Diagnostics and Life Science Industry
The Quality System Manager is responsible for ensuring proper management and leadership of all activities associated with regulatory affairs and quality compliance issues (Products, certifications, audit, suppliers, new ops reprocessing activities, instruments refurbishment projects, DC development, 3rd party logistic management, etc.) with our Corporate partners and markets partners for EMEIA.
- Quality System Manager
- Medical Devices - German
We are looking for a Regulatory and Clinical Affairs Manager
- Regulatory and Clinical Affairs Manager
- Medical devices Class III