Lead Regulatory Affairs Specialist

Nuvasive Inc

Regulatory premarket applications
510(k) submissions
Ide/pma submissions
The Lead Regulatory Affairs Specialist oversees the preparation and submission of regulatory premarket applications

Job Summary

  • The Lead Regulatory Affairs Specialist oversees the preparation and submission of regulatory premarket applications.
  • This position requires a strong understanding of regulatory requirements throughout the product lifecycle.
  • The company values teamwork and is passionate about innovation to improve patient care.

Matching Summary

The Lead Regulatory Affairs Specialist oversees the preparation and submission of regulatory premarket applications.

Skills & Requirements

Must-have

  • Regulatory premarket applications
  • 510(k) submissions
  • IDE/PMA submissions

Nice-to-have

  • Strong sense of responsibility
  • Ability to perform under pressure
  • Effective in building relationships

Key Requirements

  • Minimum of 8 years related experience
  • Bachelor’s degree or higher
  • Knowledge of FDA regulations

Work Rights

Not specified

Tailored Resume

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