Job Summary
A company is looking for a Regulatory Affairs Specialist.
Key Responsibilities
- Assist with compiling, preparing, reviewing, and submitting regulatory submissions to authorities in and outside the US
- Maintain regulatory shipping authorization documentation and prepare annual licenses and registration renewals
- Collaborate with internal teams to ensure compliance with applicable standards and interpret regulatory requirements
Required Qualifications
- Bachelor's degree and a minimum of 2 years of related experience, or an advanced degree without experience
- Working knowledge of domestic and international regulatory guidelines, policies, and regulations
- Ability to manage multiple priorities in a fast-paced environment
- Experience with pre- and post-market medical device submissions
- Proficiency in MS Word, Excel, Adobe, and PowerPoint
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