Job is Expired
Location: Illinois, Minnesota, New York, North Carolina, Wisconsin
Compensation: To Be Discussed
Staff Reviewed: Thu, Jan 14, 2021
Job Summary
A medical manufacturing company is in need of a .
Individual must be able to fulfill the following responsibilities:
- Providing global performance and safety requirements as an input to product design teams
- Managing registration plans through collaboration with global RA peers
- Reviewing product labeling including advertising and promotional material for compliance
Qualifications for this position include:
- Ability to travel 10% of the time
- Bachelor's degree
- Minimum 5 years’ experience
- Experience with FDA 510K submissions
- Proven ability to contribute creative yet practical solutions to problems
- Strong project planning, leadership, negotiation and presentation skills
