Job Title: Senior Technical Regulatory Affairs Associate
Industry: Medical Devices
Location: Cheshire
Position Type: 12 Month Fixed Term Contract (Potential for Perm)
About The Company
A world-leading developer and manufacturer of tissue-healing technology, this company focuses on quality patient outcomes and value for payers. Its surgical products include tissue adhesives, sutures, haemostats, fixation devices, and sealants. Since 2019, it has acquired seven companies specialising in internal sealants, biomaterials, wound care, and surgical implants. Products are manufactured across Europe, Asia, and Israel, with global distribution through partners and direct sales teams. The company operates R&D hubs in the UK, Ireland, Germany, France, and Israel and employs over 1,500 people.
Job Description
Overview
In this role, you will be responsible for supporting the regulatory affairs function within the medical device industry, leveraging your strong scientific background and hands-on experience with DHF (Design History File) maintenance, risk management processes, and technical regulatory submissions. You will work collaboratively with cross-functional teams to ensure compliance with global regulatory requirements, providing critical input for technical documentation, risk management, and change assessments....