Job Summary
A health technology company is in need of a Remote Regulatory Affairs Specialist II.
Core Responsibilities Include:
- Preparing post-market submissions
- Developing regulatory tactics for submissions and registrations
- Enhancing proficiency in core market
Applicants must meet the following qualifications:
- US work authorization is a precondition of employment
- BS degree in a relevant field
- 2+ years of medical device experience with BS degree, and work experience in Regulatory, R&D, Quality or clinical
- Considered a key regulatory point person in a scientific or technical discipline
- Can be trusted by Regulatory Affairs management as an independent regulatory core team member on project teams
- Strong organizational skills and time management skills
