Postes de Santé & Sciences de la Vie - Affaires règlementaires
6 offre(s) d’emploi correspondant(es)
This position will oversee development, formulation and implementation of policies, systems, strategic plans/objectives for the management of manufacturing product quality and systems, including establishment of appropriate quality and regulatory metrics to measure product quality and effectiveness of the quality and regulatory system.
- Global Quality and Regulatory
- Medical Technology
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