Regulatory Affairs Engineer

An exciting opportunity has arisen with a leading global supplier for Medical Devices. They are seeking someone with Regulatory Experience in Medical Devices to continue the companies progression in there Sussex HQ. 

Below is a brief description.

Purpose of role – Responsible for maintaining and supporting promotion of regulatory affairs and supporting overall regulatory compliance. The position provides and contributes to the delivery of regulatory deliverables from internal R&D (research and development) projects, contributing to provide regulatory solutions to business requirements and changes to regulatory landscape. The position provides operational regulatory input and guidance to cross functional terms, ensuring compliance MDSAP (medical device single audit programme) and other applicable global regulatory standards. Furthermore, the Regulatory Affairs Engineer is responsible for the completion of global regulatory submissions for product registrations in line for business to growth.

Reports to – Head of Quality Assurance and Regulatory Affairs

Accountabilities

-Prepare submissions / compliance strategy documents in line with agreed timeframes.

-Support Generation and completion of technical documentation in line with agreed timeframes

-Hands on in the remediation of technical files with agreed timeframes

More information is available on request.

Christian Lee

christianlee@barringtonjames.com

01293 776644