A company is looking for a Regulatory Affairs Specialist.
Key Responsibilities
Support regulatory registration efforts for medical devices in global healthcare spin-offs
Evaluate product changes for rebranding and their impact on existing licenses with Health Canada
Update technical documentation and coordinate with international regulatory teams for timely submissions
Required Qualifications
Bachelor's Degree or higher in Biology, Chemistry, Pharmacology, Biochemistry, or a related field
2-3 years of experience in regulatory affairs within the medical device industry
Direct experience with submissions to Health Canada
Proven ability to author technical documentation and support international registrations
Regulatory Affairs Specialist • Atlanta, Georgia, United States
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