. · Experienced quality and regulatory professional with working knowledge of ISO9001 and MDD / MDR. · Experience of working...
for planning and conducting audits of medical devices to EU MDD 93/42/EEC, EU MDR 2017/745, Directive 93/43/EEC equivalent to UK... Technology. Knowledge of: Medical devices (active, non-active or software) and Medical device management systems. EU MDD 93...
Work Model: Hybrid About the Company Tracing its roots back to 1933, MDD is one of the world’s top forensic accounting... on 5 continents, MDD has global resources to assist our clients with their forensic accounting needs. MDD helps insurance...
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...