by Clinical Affairs. The candidate will ensure clinical trial conduct in compliance with applicable laws regulations MDD/MDR...
medical device regulations Medical device industry experience including strong working knowledge and experience with MDD...
by Clinical Affairs. The candidate will ensure clinical trial conduct in compliance with applicable laws regulations MDD/MDR...
required for MDD registration. To maintain spare parts and tools store and advise the National Maintenance Manager on stock level...
internal and external regulatory requirements (including but not limited to Site, Division, Corporate, FDA, ISO, MDD...
Device Directive (MDD) / Medical Device Regulation (MDR) ISO13485 with experience on medical devices. Personal...
, MDD/MDR, CMDR, MDSAP, and all other applicable regulations. Able to professionally negotiate and lead meetings (eg Pre...
and experience with MDD and MDR Technical writing experience. Has experience evaluating manufacturing changes for impact on global...
devices (GCP/ IRB/EC / FDA & ISO standards/ EU MDD/MDR, etc.) and applies under direction of clinical management. Actively...
to take your career to the next level? If you have a strong background as a Product Assessor within an EU notified body conducting MDD/MDR.../Technical File Reviewer within another Notified Body for active devices, conducting reviews against MDD and/or MDR...