Senior Regulatory Affairs Specialist

Medtronic UK

Nanakramguda, India
Regulatory information management system
International regulatory submissions
Premarket documents for global registrations
You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world

Job Summary

  • You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
  • Responsibilities may include the following and other duties may be assigned: Set up new process for entering new data - Regulatory Information Management System.
  • Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.

Matching Summary

You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

Skills & Requirements

Must-have

  • Regulatory Information Management System
  • international regulatory submissions
  • premarket documents for global registrations
  • regulatory compliance recommendations
  • regulatory impact assessments

Nice-to-have

  • flexible and team-oriented attitude
  • self-motivated and positive
  • establish credibility with all levels

Key Requirements

  • 7+ years experience in medical device/pharmaceutical RA
  • Bachelor's degree in Life Science or related
  • Works independently with general supervision

Work Rights

Not specified

Tailored Resume

Cover Letter