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...
, 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...
to clinical sites Initiate and manage documentable compliance actions Conduct regular data quality reviews with principal... study teams throughout study protocol development and execution Appropriately engages Applied Research, Medical Affairs...