Regulatory Affairs Strategist

1 week ago


Deeside, Flintshire, United Kingdom ConvaTec Full time
About the Role

ConvaTec is a global medical products and technologies company, focused on solutions for the management of chronic conditions.

Job Summary

We are seeking an experienced Regulatory Affairs Specialist to drive improvements in regulatory affairs processes, systems, and infrastructure while supporting regulatory strategy and registration across global markets.

Main Responsibilities
  • Generate and execute regulatory strategies for phased launches of newly developed products, changed devices, and other major projects.
  • Request support from internal and external stakeholders across multiple processes, including global regulatory activities such as Renewals, Re-registrations, and Change submissions.
  • Support the business with the implementation and execution of a comprehensive regulatory intelligence system and supporting services.
Key Requirements
  • Lifescience degree or equivalent.
  • RAPS Certification preferred.
  • Regulatory/Quality experience in medical devices.
  • Experience dealing directly with Notified Bodies and global regulatory authorities.
What We Offer

As a Regulatory Affairs Specialist at ConvaTec, you will have the opportunity to work on a wide range of projects and contribute to the development of our regulatory strategies.

Our team is dedicated to providing high-quality medical products and services that make a real difference in people's lives.

We offer a competitive salary, benefits package, and opportunities for professional growth and development.

The estimated salary for this role is $95,000 - $120,000 per annum, depending on location and experience.



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