regulatory activities required to maintain compliance to US FDA, Health Canada and EU IVD Regulations (EU) 217/46, as well... as other country regulatory agencies. Represents regulatory on design teams, prepares regulatory plans, authors US FDA 510(k)s, Health...
- whatever your ambitions. About the role: The Corporate Clinical Quality Assurance (CQA) Principal Specialist will manage Corporate CQA..., or Regulatory Affairs Medical device industry experience required Extensive knowledge of FDA, ISO, EU MDR, and medical device...
– whatever your ambitions. About the role: The Corporate Clinical Quality Assurance (CQA) Principal Specialist will manage Corporate CQA..., or Regulatory Affairs Medical device industry experience required Extensive knowledge of FDA, ISO, EU MDR, and medical device...
-functional teams including Regulatory Affairs, Design, Quality and Lifecycle to ensure labeling updates are accurate, compliant... with Regulatory Affairs (RA) to verify labeling text, graphics, layout, and symbols for accuracy, completeness, and compliance...
, we recognize, develop, and empower talent! Position: Clinical Specialist, Wellness Department: Regulatory for Braun & Vicks... expectations. What you will be doing: The role will be reporting to the Senior Manager of Regulatory & Clinical Affairs. The...
does not have direct reports. Principal Contacts & Purpose of Contact Internal – Medical Affairs, Clinical Operations...://www.convatecgroup.com Convatec is looking for a senior electronic Trial Master File (eTMF) specialist who...