Medical Technology Jobs

Johnson & Johnson MedTech · Paris, France

Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of J&J products. Provides clinical expert support to HCPs, manages MIR responses within four days, and produces performance statistics with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

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.

Smith & Nephew · Stoke-on-Trent

Field-based clinical specialist role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Combines hands-on clinical support, education of community healthcare professionals, relationship building and territory management to drive adoption of therapies such as NPWT.

Smith & Nephew · London

Repair and maintain medical devices, performing preventative maintenance for service-contract customers and precision instrument servicing under a microscope, including sharpening surgical instruments. The role involves managing personal inventory, supporting the wider Service Engineering team, and building relationships with hospital staff and internal sales teams, with training to certify across multiple product franchises.

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.

Medtronic · London · £95,200 – £142,800 pa

Builds and maintains the internal platform tooling that other engineering teams rely on, spanning Infrastructure as Code with OpenTofu, EKS and Helm, CI/CD automation, and observability with OpenTelemetry. Also supports AI agentic workflows and designs pragmatic fixes for developer productivity gaps, mentoring engineers across the organisation.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

SoCode · Cambridge · £400 – £500 pd

Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.

HAYS Specialist Recruitment · Oxford

Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.

Talentmark · Welwyn Garden City · £38 – £60 ph

Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.

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.

HCRG Care Group · Runcorn · £30,000 pa

Supports and maintains clinical systems, acting as subject matter expert for TPP SystmOne, handling complex incidents, configuration queries, record management and workflow issues. Also trained to become the organisational expert for Hybrid Mail, providing second-line support. Based at a local office with remote support and occasional travel.

Johnson & Johnson MedTech · London

Supports the Medical Affairs team with intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise product use. Provides clinical expert support to healthcare professionals on post-operative outcomes, new product introductions, demos and clinical studies, working closely with Product Safety, Marketing, R&D and Commercial. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Limerick, Ireland

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Collaborates with product safety, marketing, R&D and commercial teams, providing expert support to healthcare professionals and internal customers on new product introductions. Home-office based with up to 20% travel across EMEA.