MDM Quality/Regulatory Affairs
Letzte Aktualisierung: 26.03.2020
Aufgabenbeschreibung und Anforderungen
Our international client in Baden-Württemberg is looking urgently for an Interim MDM to support their team to further success. Your Profile Expert knowledge in Regulatory Affairs and Quality in the medical device industry A natural leader, able to create and lead training programmes Experience as MDM Experience in UDI/Labelling Familiarity with MDR guidelines, IFU, VDI, Labelling and Change Management Knowledge of Agile & RA systems Experience with FDA Audits considered a plus German speaking, English is preferred This is a freelance full-time role so a capacity of 40 hours per week is required. Search terms: Regulatory Affairs, MDR, R&D, VDI, IFU, Labelling, RA Manager, IT, IT systems, Lean six sigma, FDA, contract, , ISO, ISO 13485, GCP, CAPA, GMP, QC, QM, Quality, Quality control, quality, QAM, GDP, Distribution, Pharma, GMP, SOP, Regulatory Operations, eCTD, Change Management Disclaimer: We operate as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age and experience, and we confirm that we are happy to accept applications from persons of any age and experience for this role.