Medical Technology Jobs

Johnson & Johnson MedTech · Blackpool

Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.

Johnson & Johnson MedTech · Zug, Switzerland

Supports Clinical Risk Management operational excellence by coordinating process optimisation and the day-to-day administration of the CRM digital landscape. Acts as operational point of contact for super-user forums, vendor coordination, digital asset administration, taxonomy and metadata stewardship, portal support and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.

Smith & Nephew · Wrexham

Field-based clinical sales role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Involves hands-on clinical support, education and relationship building with community healthcare professionals, guiding decision makers and strengthening advocacy for therapies across the territory.

Smith & Nephew · Watford

Owns the global OT cybersecurity programme across a medical technology manufacturer's worldwide manufacturing network, setting governance and embedding security into how industrial technologies are designed and operated. Leads risk management, incident response and secure modernisation aligned to IEC 62443 and NIST frameworks, influencing engineering, IT and business stakeholders without direct control of implementation teams.

Newton Colmore · Cambridge

Design and develop novel mechatronic systems for medical devices, including liquid handling machines and surgical robotic systems, within a multidisciplinary R&D team. Take concepts through iterations to manufacture, designing intricate mechanisms while owning wider system development. Complex mechatronics work is the priority; medical or biotech sector experience is valued.

Medtronic · Warsaw, Poland · PLN 88,000 – PLN 132,000 pa

Primary point of contact for customers through the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.

Medtronic · Madrid, Spain · €27,200 – €40,800 pa

Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations. Collaborates with service engineers, repair centres and logistics teams in a regulated MedTech environment, and contributes to process improvements and UAT activities.

Clearline Recruitment Ltd · Welwyn Garden City · £339 – £500 pd

Coordinate UK clinical study start-up activities and site activation, managing regulatory submissions, approvals and amendments. Liaise with NHS R&D departments, clinical sites and CROs, prepare site contracts, budgets and costing templates, and track timelines and regulatory milestones. Requires hands-on UK start-up experience with HRA, Ethics, MHRA, IRAS, CPMS and ICH-GCP knowledge.

SRG · Darlington · £49,045 – £69,045 pa

Provide senior scientific and technical leadership across complex RNA manufacturing programmes, informing technical strategy, technology selection and GMP translation. Oversee experimental studies, resolve complex challenges and work cross-functionally with technical, operations, quality, engineering and supply chain teams to deliver scalable, GMP-compatible processes.

Aspion · Reading · £45,000 – £50,000 pa

Field-based business development role selling electronic and electromechanical components across the Thames Valley and Surrey, combining key account management with new business development. You will work with design engineers and procurement teams to secure design-in specifications and manage technical sales pipelines from enquiry through to production, supported by product specialists and application engineers.

Kingston Barnes Ltd · Pilning · £32,000 – £36,000 pa

Assemble and wire high-tech semiconductor production equipment, working from electrical drawings to solder, crimp and loom complex panel configurations. The role sits in a production team building cutting-edge systems and also involves fault finding and implementing corrective action. Double day shifts with an early Friday finish.

Healthium Clinics · Henley-on-Thames · £35,000 pa

Supports market access, quality systems and governance across healthcare and technology activity, coordinating evidence packs, tenders and regulatory documentation. Maintains the Quality Management System, risk registers and audit actions, and monitors MHRA, CQC, NICE and ICO requirements. Works with clinical, technical and commercial colleagues to keep registrations and controls inspection-ready.

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.

GE HealthCare · United Kingdom, YY9 9YY

Provides day-to-day medical oversight for one or more clinical trials, ensuring patient safety, data integrity and protocol compliance. Reviews and assesses AEs and SAEs, supports safety signal detection with Pharmacovigilance, and advises investigators on eligibility and dosing. Works cross-functionally with Clinical Operations, Data Management, Biostatistics and Regulatory Affairs, and contributes to CSRs and regulatory submissions.