Teams at Vision RT

Investigates and classifies medical device complaints, performs root-cause analysis, supports reportability decisions and risk assessments, and prepares regulatory reports. The role collaborates with Quality, Regulatory, Production, R&D, Service, and external stakeholders; supports audits; and becomes qualified to conduct internal audits against ISO 13485, MDSAP, EU MDR, and potentially ISO 9001. Occasional UK and international travel is required.

Provide clinical support, training, technical guidance, product demonstrations, workflow documentation, and testing for Vision RT radiotherapy systems across EMEA. The role supports customer adoption, sales teams, distributors, conferences, software releases, and R&D feedback while requiring substantial travel across UK customer sites.

Lead regulatory affairs and quality management for Vision RT Shanghai, including Class III medical device registrations, NMPA liaison, post-market surveillance, adverse event and field action reporting, audits, licensing, and QMS compliance. The role serves as the Shanghai quality representative and requires fluent Mandarin, strong English, ISO 13485 and NMPA expertise, plus China and international travel.