In this role, you will determine current regulatory requirements and strategies for Terumo Medical Corporation and Terumo Corporation projects. Defines information and actions necessary to meet these requirements.
The Regulatory Affairs Specialist - Medical Device will need experience with supporting the legal department in a wide range of matters, including litigation, compliance, and corporate transactions for all commercial/business claims with due diligence.
In this role, you will be responsible for ensuring compliance to include adherence to DEA regulations regarding controlled substances, State regulations of controlled substances and prescription drugs, internal due diligence policies and in cross - training in all aspects of the Regulatory Compliance department.
In this role, you will develops, designs, manages and integrates Beckman Coulters regulatory strategies and programs.collaborates with the regulatory staff from other business units, companies, government agencies and Product Regulatory Subcommittees to develop harmonized policies, procedures and work instructions for emerging regulatory topics.