Senior Regulatory Affairs Specialist
Smith & Nephew(18 days ago)
About this role
Smith+Nephew is seeking a Senior Regulatory Affairs Specialist to manage regulatory submissions, develop strategies, and ensure compliance for medical devices. The role involves collaboration across teams to support product launches and market expansions globally.
Required Skills
- Regulatory Submissions
- Medical Devices
- ISO13485
- GMP
- Regulatory Strategy
- 21 CFR 820
- EU MDR
- Technical Documentation
- Project Management
- Regulatory Compliance
About Smith & Nephew
smith-nephew.comSmith+Nephew is a global portfolio medical technology business. We design and make technology that takes the limits off living.
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