244 jobs
Johnson & Johnson MedTech Spring House, United States US$109,000 – US$174,800 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Executes system improvements, study build and maintenance, end-user support, release management, UAT and integrations, and explores automation, analytics and GenAI opportunities. Also delivers training and supports audits and regulatory inspections.
Johnson & Johnson MedTech Raritan, United States US$109,000 – US$174,800 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and audits, while driving automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.
Medtronic London £100,000 – £150,000 pa
Leads global cross-functional teams to design, implement and commercialise digital, electro-mechanical and robotic medical devices, managing multiple complex hardware and embedded software programmes from initiation through delivery. Involves risk management, requirements planning and reporting to executive leaders, using waterfall, Scrum and Agile methods in a highly regulated, safety-critical environment.
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.
Medtronic London £76,800 – £115,200 pa
Designs, builds and maintains AWS and on-prem infrastructure used by ML engineers, data scientists and product teams, with a strong focus on Kubernetes, GitOps, Terraform and Docker. The role sits in the Surgical AI Centre of Excellence, supporting an MLOps platform for connected operating-room products, and requires two days a week in London.
Gold Group Falmouth
Hands-on R&D role designing and improving electro-mechanical medical devices for women's health and fertility, covering schematic capture, PCB layout in Altium, verification and validation testing, EMC and IEC 60601 electrical safety compliance, and hardware/software integration. Works within a collaborative international R&D team on both new product development and sustaining engineering, with prototyping, debugging and technical documentation duties.
SoCode Cambridge £40,000 – £50,000 pa
Hands-on electronics design role at a product development consultancy, owning hardware at system and circuit level from concept through prototyping, debug, verification and into production for medical and healthcare clients. Work spans medium and high-volume manufacture in well-equipped labs, with peer review across disciplines and a new technical challenge every few months.
Avanti Recruitment ELY £65,000 – £75,000 pa
Hands-on R&D role developing advanced sensing and measurement technology, owning electronics from concept and architecture through PCB design, prototype bring-up, testing and production. Focus on low-noise analogue and mixed-signal electronics alongside high-speed digital, FPGA and microcontroller hardware, with signal integrity work on complex multi-layer boards.
Vertech Group (UK) Ltd London £75,000 – £85,000 pa
Assesses software development processes and technical evidence for AI-enabled medical devices, reviewing lifecycle, V&V, configuration management and risk to determine whether safety-critical products meet certification standards. Uses AI-assisted tools to explore evidence, identify failure modes and flag inconsistencies within a specialist team.
Real Tipperary, Ireland £52 – £60 ph
Supports the development and improvement of complex medical devices within a multidisciplinary engineering team, covering the full product lifecycle from concept and mechanical design through prototyping, testing, verification, validation and commercial launch. Also involves failure investigation, sustaining engineering, design improvements and compliant design and risk-management documentation.
TRS Consulting Reading £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 company car.
TRS Consulting Milton Keynes £45,000 – £55,000 pa
Home-based account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. Involves managing key customer accounts, identifying new business, attending exhibitions and local events, analysing competitor activity and producing proposals and sales agreements to exceed area sales targets.
Platform Recruitment London
Develops and optimises therapeutic delivery formulations, running lab-based in vitro studies and analytical characterisation to assess stability and performance. Works in a multidisciplinary team progressing early-stage technologies toward manufacturing, with external partner collaboration and scale-up considerations.
Reed Stroud £58,000 – £63,000 pa
Lead packaging and labelling validation for medical devices, managing transportation testing, shelf-life studies and equipment validation projects. Review technical documentation, BOMs and labelling content, drive process improvements, and lead non-conformance and CAPA investigations. Act as key contact during internal, customer and regulatory audits, supporting regulatory submissions and mentoring junior team members.
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.
