Senior Regulatory Specialist

Nuvasive Inc

5+ years of regulatory experience
Knowledge of fda regulations
Experience with 510(k) submissions
The Senior Regulatory Affairs Specialist plays a crucial role in drafting and submitting FDA submissions for medical devices

Job Summary

  • The Senior Regulatory Affairs Specialist plays a crucial role in drafting and submitting FDA submissions for medical devices.
  • This position requires collaboration with product development teams to ensure timely submissions.
  • Globus Medical is committed to improving patient care through innovative solutions.

Matching Summary

The Senior Regulatory Affairs Specialist plays a crucial role in drafting and submitting FDA submissions for medical devices.

Skills & Requirements

Must-have

  • 5+ years of regulatory experience
  • Knowledge of FDA regulations
  • Experience with 510(k) submissions

Nice-to-have

  • Strong communication skills
  • Ability to work under pressure
  • Team-oriented mindset

Key Requirements

  • Bachelor's degree or equivalent experience
  • Understanding of product lifecycle regulations
  • Ability to evaluate regulatory impacts

Work Rights

Not specified

Tailored Resume

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