Medical Technology Jobs

Johnson & Johnson MedTech · Raritan, United States · US$102,000 – US$177,100 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors performing anonymisation and synthetisation, serves as the primary contact for YODA Project requests, and supports external research teams using clinical study data. Operates independently as a subject matter expert within the Clinical Data Standards and Transparency team.

Johnson & Johnson MedTech · High Wycombe

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.

Smith & Nephew · Hull

Acts as a key technical resource supporting manufacturing operations through automation, controls and machine connectivity solutions. Drives Smart Factory capabilities, resolves production issues and promotes cybersecurity best practices across OT systems at multiple sites, liaising between the OT Centre of Excellence and plant operations.

Smith & Nephew · Swansea

Field-based sales role covering South Wales, Cheltenham, Gloucester and Worcestershire, owning key hospital and community accounts for Sports Medicine products. You build strategic account plans, run quarterly business reviews, develop tailored proposals and use CRM data to grow revenue and market share with NHS stakeholders.

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.

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.

SPD Development Company Ltd · Bedford

Provides statistical expertise across R&D, Clinical, Product Support and Marketing, designing and analysing studies and supporting product algorithms and evidence generation. Sits in a three-person Statistical & Data Services Team, acting as statistical representative on assigned projects and communicating findings to technical and non-technical audiences.

Johnson & Johnson MedTech · Stockholm, Sweden

Supports the Medical Affairs team for intraocular lenses, analysing surgical cases and calculations, managing medical information requests within four days, and helping clinicians optimise post-operative outcomes. Works closely with Product Safety, Marketing, R&D and Commercial on clinical performance reporting and new product introductions, with home-office working and up to 20% travel.

Johnson & Johnson MedTech · Pomezia, Roma, Italy

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

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.