200 jobs
Johnson & Johnson MedTech Toronto, Canada US$134,000 – US$184,000 pa
Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned programmes, planning and directing writing groups, mentoring junior writers and overseeing external contractors. Also manages direct reports, setting objectives and running performance and development discussions.
Johnson & Johnson MedTech Allschwil, Switzerland
Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Acts as lead writer or point of contact for assigned programmes, planning and directing writing groups while coaching junior staff and managing direct reports. Involves cross-functional collaboration, regulatory guideline knowledge and departmental process improvement.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing a wide range of biomedical devices across a London patch, with occasional UK travel and 2-3 overnight stays per month. The technician receives manufacturer-funded training to become certified on high-complexity medical lasers, with progression into more senior positions. Working Monday to Friday, 40 hours per week, with time off in lieu for excess hours.
TRS Consulting Birmingham £45,000 – £55,000 pa
Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets.
TRS Consulting London £45,000 – £55,000 pa
Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets. Home-based with a territory focus.
Medtronic London £77,040 – £115,560 pa
Serves as a senior scientific expert for the Neuromodulation & Pelvic Health portfolio, leading external scientific engagement with KOLs, healthcare professionals and medical societies across Western Europe. Delivers evidence-based clinical information, runs advisory boards, CME programmes and congress activities, and partners with clinical, regulatory and commercial teams on medical affairs strategy. Remote UK-based role with frequent travel.
Spire Healthcare Elland
Operational lead for the hospital's medical device management programme, acting as subject matter expert for equipment lifecycle, maintenance, asset control and regulatory compliance. Day to day involves managing biomedical equipment work orders, liaising with clinical departments and third-party engineers, training staff and running asset tagging and quarantine checks.
Optical Express South East England £40,000 pa
Lead the internal audit programme across a regional network of clinics, conducting on-site compliance audits against HIS, CQC, HIW and RQIA standards and working with local managers on corrective action plans. Deliver regulatory guidance, training and policy support, reporting findings to senior leadership and the Director of Care & Quality. Involves regular travel across the Midlands and South of England.
Optical Express East Midlands £40,000 pa
Lead the internal audit programme across a network of clinics, conducting on-site compliance audits against HIS, CQC, HIW and RQIA standards and working with local managers on corrective action plans. Provide regulatory guidance, deliver training, and report compliance status to the Director of Care & Quality, with regional travel across the Midlands and South of England.
Russell Taylor Group Deeside £29,000 – £34,000 pa
Supports diagnostic testing, assay development and IVD kit manufacture within an established scientific team. Day-to-day work includes processing client samples, operating PCR and capillary sequencing equipment, running quality control checks and managing stability storage. Also involves data analysis, report writing and taking ownership of assigned projects.
Matchtech Fareham
Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.
Randstad Construction & Property London
Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.
Automated Industrial Robotics Wakefield
Designs special purpose machinery from concept through to production-ready drawings, working with AutoCAD 2D/3D and pneumatic and electrical components. Manages schedules, budgets and scope changes while liaising with the Technical Director and section leads, and conducts machinery risk assessments and detail checks on colleagues' work.
Oxford Nanopore Technologies Oxford
Join the Biologics Tech Transfer team to support the onboarding and scale-up of production for analyte and other components used in sequencing kits. The role centres on transferring and scaling biological production processes within a biotech manufacturing environment.
Oxford Nanopore Technologies Oxford
Runs sequencing experiments across the full range of Oxford Nanopore platforms to assess new developments and set performance expectations. Sits within the Product Validation team, working hands-on with sequencing technology to characterise platform capabilities.
