Job Summary
A professional services firm is filling a position for a Remote Senior Medical Device Regulatory Affairs and Advertising Promo Specialist.
Individual must be able to fulfill the following responsibilities:
- Prepare FDA submissions including PMA submissions
- Influence and inspire alignment with business goals, internally and externally
- Participate in project meetings and provide feedback to product development teams
Applicants must meet the following qualifications:
- 8+ years of relevant regulatory affairs experience
- Maintain proficiency in worldwide regulatory requirements
- In depth understanding of the essentials of advertising and promotion law
