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Principal Regulatory Affairs Specialist
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Full-time
- Together, we can change healthcare worldwide.
- As Principal Regulatory Affairs Specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies.
- Working with global Regulatory Affairs colleagues, you will ensure submissions are accurately prepared and comply with global regulations.
- In this role, you will have primary RA responsibility for multiple Class II (IIa/IIb) and Class III products, working within a collaborative team environment that fosters professional development while focusing on meeting business objectives with excellence.
- Team with business unit Regulatory Affairs Specialists (RAS) to provide regulatory support for new product introduction (NPI) and marketed products under MDD and MDR Regulation.
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