Position Details
Regulatory Affairs Manager Apply
Regulatory Affairs Manager
Location: St. Paul, MN
Duration: 6 months
Shift: 8 am to 5 pm
Key Highlights of the Role:
Required Experience: 9+ years in regulatory affairs, with significant experience in FDA and EU MDR submissions for Class III medical devices
Skills & Qualifications:
- Strong leadership, organizational, and communication skills
- Proven track record with FDA, EU MDR, and other global regulations
- Expertise in managing regulatory submissions and approvals for medical devices
- Ability to work effectively in cross-functional teams
