Affairs, Medical Advisor Pipeline (MAP) and other internal stakeholders, as needed. Following quality issue processes... and regulatory inspections in liaison with PMCO, SML, COLM and Quality Group. Profil You will need to have: Minimum of 4 years...
. Profil We are targeting profiles that have a strong background in quality management and regulatory affairs and that have a demonstrated... a plus. 4+ years of relevant experience in quality management and regulatory affairs for medical devices. Prior proven...
, authentic and useful. Job Description Lead and manage the Clinical Affairs team, covering clinical evaluation/validation... with EU MDR, FDA and other regulatory requirements Work cross-functionally with R&D, Marketing, Sales, Product Management...
... Job Title: Executive Director (m/f/x), Quality Management System R&D & PV QA Posting Start Date: 24/10/2025... Job Description: For our Daiichi Sankyo European Headquarters (in Munich), we are looking for a Executive Director (m/f/x), Quality Management System...