Regulatory Affairs Specialist in Leeds - X4 Life Sciences

Job Description A long term Medical Device client of ours based in West Yorkshire, are looking to add a Regulatory Specialist to their team to support their growing business.

They are looking for an individual that is hard working and self-motivated to assist with all things regulatory. Responsibilities will include:

Provide technical support to the business, suppliers and customers on all matters relating to the safety, legality and quality of the products purchased and sold.
A clear understanding of the legal requirements for labelling and testing within the required product areas.
To ensure all products comply with relevant legislation.
Produce and maintain up to date technical files for medical devices to the required standards.
Ensure all quality and technical issues relating to technical files are resolved effectively. Escalate when necessary to the Technical Manager/Director
Assess device related incidents/complaints for medical device reporting requirements. When required, compile and submit reportable events to relevant regulatory authorities in timely manner.
Review of complaint and other product related information in order to create annual Post Marketing Surveillance report.
Support the introduction of New products by advising on Regulatory requirements when appropriate.
Perform Mock recalls as necessary.

Competencies:
3 years experience in Medical devices (class I and IIa).
Experience in Technical files and Post market surveillance.
Expert knowledge of MDR, ISO13485, UK MDR.
Experience interacting with Notified/Approved Body.

Please share your CV at e.smailes@x4lifesciences.com if you are interested in hearing more about the position. As always if anyone in your network may be a good fit, please share their details as we offer a referral bonus upon the successful placement.