Job Summary
A company is looking for a Director, Cybersecurity Regulatory Affairs.
Key Responsibilities
- Interface with clients to gather information and ensure compliance with regulatory guidelines for submission documentation
- Conduct risk management and vulnerability analyses on medical devices and support cybersecurity strategy development
- Research and report on industry best practices and evolving cybersecurity standards to enhance client services
Qualifications
- Bachelor's degree in engineering, science, information systems, or a related field; advanced degree preferred
- 6-8 years of experience in Regulatory Affairs related to medical devices, including writing/reviewing US regulatory submissions
- 5+ years of experience in information/cyber security
- Understanding of medical device development concepts and technical background in software and cybersecurity strategies
- Fluency with FDA regulations and experience with pre- and post-market management of cybersecurity guidance documents preferred
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