Medical Technology Jobs

Johnson & Johnson MedTech · Blackpool

Performs physical, analytical and chemical QC testing on raw materials, in-process and finished products, and leads laboratory and non-conformance investigations. The role covers GMP documentation, equipment calibration, method validation and consumable management while ensuring compliance with ISO 13485, ISO 14001 and FDA QMSRs. It also involves training other staff and liaising with approved manufacturers to keep testing on schedule.

Johnson & Johnson MedTech · Maidenhead

Oversees local UK clinical trials from start-up through database lock, acting as the country-level point of contact and coordinating the local trial team to deliver compliant, high-quality data. Leads feasibility, site selection, recruitment planning and IRAS submissions, while mentoring CTAs and Site Managers and monitoring trial progress against timelines and budget.

Smith & Nephew · Luton

Owns and grows a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Drives new business, account plans, tenders and adoption of advanced technologies including robotics, working alongside Account Managers and Area Business Managers.

Smith & Nephew · Peterborough

Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Combines clinical expertise with commercial account planning, tenders and product introductions, including advanced technologies such as robotics.

Medtronic · London · £76,800 – £115,200 pa

Develops high-performance, low-latency video and AI processing pipelines for use in the operating room, leveraging hardware acceleration for capture, inference, visualisation and streaming. Works in a multidisciplinary team on safe-by-design medical device software, optimising real-time pipelines with C++17-23, multi-threading and inter-process communication. Requires two days per week onsite in London.

Johnson & Johnson MedTech · Breda, Netherlands · €64,000 – €103,040 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Hybrid role with up to 10% travel.

Johnson & Johnson MedTech · Leiden, Netherlands · €64,000 – €103,040 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, release management, UAT, integrations, end-user support and audits, and drives automation, analytics and GenAI improvements. Hybrid working with up to 10% international travel.

Johnson & Johnson MedTech · Spring House, United States · US$109,000 – US$174,800 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Executes system improvements, study build and maintenance, end-user support, release management, UAT and integrations, and explores automation, analytics and GenAI opportunities. Also delivers training and supports audits and regulatory inspections.

Johnson & Johnson MedTech · Raritan, United States · US$109,000 – US$174,800 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and audits, while driving automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.

Johnson & Johnson MedTech · Beerse, Belgium · €72,500 – €115,230 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.

Johnson & Johnson MedTech · Horsham, United States · US$109,000 – US$174,800 pa

Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, release management, user acceptance testing, integrations, end-user support and audits, while driving automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.

Johnson & Johnson MedTech · Maidenhead

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.

Johnson & Johnson MedTech · Maidenhead

Supports Clinical Trial Management Solutions including CTMS, Site Payments and Access Provisioning, acting as liaison between business partners, IT and suppliers. Handles study build, system integrations, release management, user acceptance testing, end-user support and audits, while identifying automation, analytics and GenAI improvements. Requires deep clinical development and GCP knowledge.

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.

Johnson & Johnson MedTech · Horsham, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.