Job Summary
A company is looking for a Senior Regulatory Affairs Specialist responsible for ensuring compliance with local regulations in North America.
Key Responsibilities:
- Compile technical documents and author local regulatory submissions for FDA and Health Canada
- Provide guidance to product development teams on local product submission requirements
- Review proposed labeling changes to assess regulatory impact on existing certifications
Qualifications:
- Bachelor's Degree required, preferably in STEM/Medicine/Life Science; Master's Degree in Regulatory Affairs preferred
- 2+ years of Regulatory Affairs experience required
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