A medical software developer has a current position open for a Remote Regulatory Affairs Project Manager.
Candidates will be responsible for the following:
Leading the preparation and review of regulatory submissions to the US FDA and international regulatory authorities
Managing government interactions pertaining to medical device registrations and licensing
Qualifications for this position include:
Bachelor’s degree in Science, Engineering, Math, or medical field
6+ years of experience in medical device Regulatory Affairs
Superb analytical and excellent communication skills
