Job Summary
A company is looking for a Regulatory Affairs Specialist - Shockwave.
Key Responsibilities
- Compile, prepare, review, and submit regulatory submissions to authorities outside the US and EU
- Assist with the preparation of product registration documents and maintain regulatory shipping authorization documentation
- Review R&D, quality, preclinical, and clinical documentation for submission filing and ensure compliance with applicable standards
Required Qualifications
- Bachelor's degree and a minimum of 2 years of related experience, or an advanced degree without experience, or equivalent work experience
- Ability to work collaboratively in a fast-paced environment while managing multiple priorities
- Working knowledge of applicable domestic and international regulatory guidelines, policies, and regulations
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