Regulatory Affairs Global Regulations Specialist

Philips UK

**
10+ years regulatory affairs experience
Medical device regulatory submissions
India regulatory affairs submission expertise
** Philips UK is seeking a Regulatory Affairs Global Regulations Specialist with over 10 years of experience in medical device regulatory affairs. The role focuses on leading global regulatory monitoring, ensuring compliance, and fostering relationships with regulatory agencies while working collaboratively across teams. **

Job Summary

  • The role leads global regulatory monitoring and strategy implementation to ensure compliance with international market requirements.
  • Candidates must possess over a decade of experience specifically in Regulatory Affairs for medical devices.
  • The position requires coordinating relationships with regulatory agencies and providing strategic guidance to product teams on compliance.

Matching Summary

Match Score: 75

** Philips UK is seeking a Regulatory Affairs Global Regulations Specialist with over 10 years of experience in medical device regulatory affairs. The role focuses on leading global regulatory monitoring, ensuring compliance, and fostering relationships with regulatory agencies while working collaboratively across teams. **

Skills & Requirements

Must-have

  • 10+ years Regulatory Affairs experience
  • Medical device regulatory submissions
  • India regulatory affairs submission expertise

Nice-to-have

  • Windchill system experience
  • Manufacturing licensing knowledge
  • Cross-functional collaboration skills

Key Requirements

  • Bachelor's degree in engineering
  • 10+ years of experience in Regulatory Affairs
  • Experience with India regulatory submissions

Work Rights

Not specified

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