Job Summary
A healthcare company is seeking a Remote Regulatory Affairs Specialist in Bedford.
Must be able to:
- Ensure continued compliance with regulatory agency approvals
- Support product development teams for new product submission requirements
- Coordinate, compile, and submit US and international regulatory filings
Must meet the following requirements for consideration:
- Excellent organizational skills
- A minimum of a Bachelor's Degree in lifesciences, engineering or related field
- 1-2 years of working experience in the Medical Device industry
- Effective written and oral communication, technical writing, and editing skills
