Medical Device Compliance Manager
3 weeks ago
Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations.
Job DescriptionThis role involves leading project submissions for regulatory approvals and acting independently to identify and resolve problems. The ideal candidate will have advanced regulatory expertise, strategic thinking, and creativity in support of programs.
Responsibilities- Lead project submissions for regulatory approvals
- Apply advanced regulatory expertise to guide cross-functional partners
- Demonstrate strategic thinking and creativity in support of programs
- Provide regulatory affairs project management for various areas
- Bachelor's degree in a medical, science, or engineering-related discipline
- 8 years of experience in the medical device industry, with 5 years related to FDA and EU MDR submissions
- Ability to work effectively on project teams
- Competitive salary: $120,000 - $180,000 per year
- Opportunities for career growth and professional development
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