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A global leader in medical technology is seeking a Regulatory Affairs Coordinator in Swindon, UK. This role involves supporting compliance and documentation practices across the EMEA region, ensuring audit readiness, and fostering continuous improvement. Responsibilities include maintaining product registrations, coordinating regulatory databases, and enhancing awareness of QA processes. Ideal candidates have at least 1 year of administrative experience and strong communication skills.
Company Overview
CONMED is a global leader in medical technology, dedicated to developing and delivering surgical and patient monitoring products that empower physicians to provide superior care, achieving better clinical outcomes for their patients.
Our products, recognized as technological frontrunners in their respective fields, are trusted by healthcare professionals worldwide. We serve key specialties including Orthopaedics, Laparoscopic, Robotic & Open Surgery, Gastroenterology & Pulmonology, and Cardiology & Critical Care, where the CONMED name is synonymous with quality and innovation. With a diverse portfolio designed to meet the specific needs of each specialty, we offer our customers both choice and convenience, enhancing care at every touchpoint.
Job Summary
Supports quality and regulatory practices across EMEA, with a focus on compliance and maintaining documentation, whilst fostering continuous improvement and knowledge sharing across the region.
Key Responsibilities
Essential
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.