Medical Technology Jobs

Johnson & Johnson MedTech · IE009 Janssen Cilag Ltd

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists HCPs with post-operative outcome analysis. Provides clinical expert support for new product introductions, demos and clinical studies, working home-office based with up to 20% travel.

Johnson & Johnson MedTech · Roden, Netherlands

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists HCPs with post-operative outcome analysis. Provides clinical expert support for new product introductions, demos and clinical studies, working home-office based with up to 20% travel.

Vero Hr · Cambridge · £45,000 – £55,000 pa

As a Quality & Regulatory Specialist, you will support clients in developing medical devices with a strong software focus, ensuring they meet regulatory requirements and quality standards. Your role involves creating and reviewing technical documentation, educating clients on regulatory needs, and collaborating with software engineers and senior stakeholders to deliver practical solutions.

Morgan McKinley · Bampton · CA$40,000 – CA$50,000 pa

Hands-on role bridging R&D and production for next-generation fluidic products, building, wiring and commissioning assembly fixtures, automated test equipment and robotic cells. Involves process scale-up (precision dispensing, laser welding, leak testing), equipment validation (FAT/SAT, IQ/OQ/PQ) and continuous improvement using root-cause analysis and SPC. Works alongside senior engineers in a fully on-site manufacturing environment.

Reed · Southampton · £28,000 – £35,000 pa

Hands-on warehouse role combining physical duties with stock control and systems work for a medical device manufacturer. You will manage inventory accuracy, goods receipt, picking and dispatch, and help develop SAP and WMS processes alongside the Operations Director. Distinct for its blend of floor work and administrative process improvement.

Optical Express · London · £40,000 pa

Leads 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. Provides regulatory guidance, designs and delivers staff training, and reports compliance status to the Director of Care & Quality. Involves regular travel across the Midlands and South of England.

Ernest Gordon Recruitment · Mitcham · £40,000 – £45,000 pa

Field-based role servicing biomedical and aesthetic laser equipment across a London patch, with occasional UK travel and roughly two nights away per month. The engineer receives manufacturer-funded training and certification on high-complexity medical lasers, with a progression plan toward senior positions. Working Monday to Friday, 40 hours per week, with time off in lieu for excess hours.

Ernest Gordon Recruitment · Andover · £40,000 – £45,000 pa

Maintains and develops the quality management system in a high-end cleanroom, ensuring compliance with ISO 9001, ISO 13485 and AS9100, with training provided where needed. Uses CAPA, 8D and 5 Whys to drive quality standards, supported by a team of six. Works Monday to Thursday 8:30am-5pm with an early Friday finish.

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.

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.

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.

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.

TRS Consulting · Oxford · £45,000 – £50,000 pa

Servicing and repairing advanced medical systems and healthcare equipment across the Oxford area, covering electronic, electrical and mechanical faults. Joining a global engineering team focused on long-term customer relationships, with manufacturer product training and a route into more technical specialist roles.

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.

Russell Taylor Group · Swadlincote · £30,000 – £34,000 pa

Supports site validation activities across cleaning, computerised systems, equipment/utilities qualification and process validation, authoring protocols and reports and interpreting data against acceptance criteria. Works cross-functionally to maintain validated status of systems and processes, investigates non-conformances and supports regulatory inspections and internal audits.