Regulatory Affairs Specialist: Medical Device Sparks United States,
Becton Dickinson (company)
The Regulatory Affairs Specialist will be responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This responsibility entails development, execution and management of procedures and systems designed to ensure that the product development process, including clinical studies, addresses all regulatory requirements as well as the objectives of the business.
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