🚀 Join the GBUK Group Team: Regulatory & Post Market Affairs Associate
🚀Are you passionate about medical device compliance, patient safety and bringing quality healthcare products to market?
We're looking for a Regulatory & Post Market Affairs Associate to join our growing team at our North Duffield headquarters in North Yorkshire.
This is an exciting opportunity to play a key role in supporting the lifecycle management of our medical devices, with responsibilities spanning:
✔ Post Market Surveillance (PMS) and Post Market Clinical Follow-Up (PMCF) activities
✔ Preparation and maintenance of PMS, PMCF and safety documentation
✔ Regulatory and technical file support
✔ Cross-functional project work with Quality, Clinical and Commercial teams
✔ Audit preparation and regulatory compliance activities
✔ Supporting innovative new product development initiatives
We're looking for someone with a scientific, medical, engineering or related background who combines strong analytical skills with exceptional attention to detail. Experience within the medical device sector is highly desirable, particularly in regulatory affairs, clinical affairs, post-market activities or quality management systems.
At GBUK Group, you'll be part of a collaborative, supportive team dedicated to improving patient outcomes through innovative medical technologies.
📍 Location: North Duffield, North Yorkshire
📩 Interested? We'd love to hear from you. The closing date for this role is 10th June and applications must be received before that date in order to be considered.
Apply now or contact us for an informal conversation about the role.