Medical Technology Jobs

Johnson & Johnson MedTech · New York, United States

As an AI/ML/Data Science Intern, you will work on developing and implementing advanced AI methods for medical image and video understanding. Your responsibilities will include conducting interviews with clinical personnel, designing and evaluating computer vision models, and extracting insights from medical imaging data to improve clinical trial efficacy.

Johnson & Johnson MedTech · Spring House, United States

As an AI/ML/Data Science Intern, you will work on developing and implementing advanced AI methods for medical image and video understanding. You will collaborate with clinical personnel to understand their needs, design and evaluate computer vision models, and communicate technical insights to diverse stakeholders.

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

Maintains and develops the Quality Management System in a high-end cleanroom, supported by a team of six. Ensures compliance with ISO 9001, ISO 13485 and AS9100, applying CAPA, 8D and 5 Whys methods, with training provided where needed. Distinct for its medical devices focus within a growing specialist manufacturer serving aerospace, automotive and medical clients.

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

Field-based role servicing 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 and time off in lieu for excess hours.

OrganOx · Oxford

Designs and develops electronic circuits and PCB layouts for medical devices, taking full lifecycle ownership from concept through to manufacturing handover. Work covers schematic capture, component selection, prototyping, debugging and verification against IEC 60601, collaborating closely with mechanical, software and systems engineers. Based on-site in Oxford with some remote design work.

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.

Newton Colmore · Cambridge

Medical Devices Consultant - Senior Mechanical Engineer - CambridgeDue to the growth of a leading Medical Devices organisation, we are currently seeking a Senior Mechanical Engineer, Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role....

Newton Colmore · Cambridge

Principal Mechanical Design Engineer - Medical Devices - CambridgeA growing Medical Devices team, based in Cambridge, is currently seeking an experienced Mechanical Design Engineer to lead the development of cutting-edge Medical Devices in the fields of Health Technology, Biotech, and...

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.

VK Recruitment · Belfast · £50,000 – £65,000 pa

Oversee complex production workflows in a specialist dental laboratory, providing technical leadership across CAD/CAM, milling, 3D printing, PMMA, zirconia and ceramics. Troubleshoot equipment and software issues, improve efficiency and quality, and coach technicians and departmental leads. Reports to the Associate Director after a structured induction.

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.

HCRG Care Group · Runcorn · £50,000 pa

Leads end-to-end data migration projects moving sensitive patient records between Electronic Patient Record systems, coordinating internal teams, external organisations and suppliers. Combines technical project management with data quality, information governance and clinical safety, working closely with the Head of Clinical Systems. Predominantly remote with occasional UK travel.

Planet Recruitment · Abingdon · £28,000 – £35,000 pa

Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.

SGS · United Kingdom · £30,000 – £32,000 pa

Coordinate and support technical documentation reviews for the UK Medical Devices team, managing review processes, monitoring KPI reports and driving resultant actions. Handle complaints, raise purchase orders for client invoicing, and strengthen key client relationships through calls and meetings. Requires practical experience of Medical Device Regulations or auditing regulations and strong documentation control.