The RAS develops and executes strategies for global regulatory approvals to introduce new and modified medical devices to the market
Job Summary
The RAS develops and executes strategies for global regulatory approvals to introduce new and modified medical devices to the market.
This role primarily focuses on regulatory support for the US and EU markets, with a wide variety of regulatory tasks to allow you to make the most of your existing knowledge base while growing your RA skill set every day.
Medtronic offers a competitive Salary and flexible Benefits Package.
Matching Summary
The RAS develops and executes strategies for global regulatory approvals to introduce new and modified medical devices to the market.
Salary
Base: $73,600.00 - $110,400.00; Bonus/Equity: MIP eligible; Benefits: Health, Dental, Vision, HSA, FSA, Life Insurance, LTD, Dependent Daycare FSA, Tuition Assistance, Simple Steps, Incentive Plans, 401(k) with match, Short-term disability, PTO, Paid Holidays, ESPP, EAP, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan
Skills & Requirements
Must-have
global regulatory approvals
regulatory submissions
post-market regulatory compliance
product changes regulatory impact
FDA and worldwide agencies
Nice-to-have
engineering concepts and scientific terminology
scientific literature evaluation
cross-functional team collaboration
presentation skills for groups
Key Requirements
Bachelor's Degree in Engineering, Life Sciences, or related
2+ years of related experience
Masters degree with 0 years of experience
US work authorization required for non-Principal roles
Work Rights
Unrestricted US work authorization for non-Principal roles