Regulatory Affairs Specialist
Baxter International(1 month ago)
About this role
A Principal Specialist in Regulatory Affairs at Baxter is responsible for driving regulatory strategy and compliance for a defined product portfolio with a focus on EU MDR and MDD. The role partners with global stakeholders and legal manufacturers to support product registrations, CE marking, and interactions with notified bodies and competent authorities.
Required Skills
- EU MDR
- MDD
- Regulatory Strategy
- Product Registration
- CE Marking
- Regulatory Submissions
- Audits
- Document Control
- TrackWise
- RIM Vault
+3 more
Qualifications
- Degree in a Relevant Scientific Field
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