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... Reviewer within another Notified Body for active devices, conducting reviews against MDD and/or MDR. Additionally...
devices Good knowledge of MDD and MDR UK / EU experience Good knowledge of ISO 13485...
, extractable and leachable data, toxicological risk assessments Working knowledge of the MDR, MDD and related ISO standards...
(ISO 13485, 21 CFR, MDD/MDR and UKCA regulations) Assist in the logging, investigating, and documenting of all non...
and remediation against regulatory documents and standard documents. Classification of medical devices based on USFDA, TPD, MDD, PAL... experience for medical device Knowledge on 21 CFR Part 820, Part 11, ISO 13485, MDD, MDR,ISO 14971 Additional Skills Previous...
with Medical Dev. Director (MDD) and other relevant Ipsen team members Lead clinical project processes: Support the CDPD... in collaboration with CDPD, MDD, GMA, CRO and Ipsen Affiliates (if needed) to identify and gain approval for high quality...
with manufacturing / production in quality control Knowledge in processes for transition from EU MDD to EU MDR...
with Medical Dev. Director (MDD) and other relevant Ipsen team members Lead clinical project processes: Support the CDPD... in collaboration with CDPD, MDD, GMA, CRO and Ipsen Affiliates (if needed) to identify and gain approval for high quality...
Our London, ON office is currently seeking a Staff Accountant to join our team. MDD, A Davies Company... considered an asset Additional languages considered an asset MDD firmly supports the development of our staff, and encourages...