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 · 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.

Smith & Nephew · Cambridge

Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, acting as clinical and commercial expert. You'll support complex surgical cases in theatre, build surgeon relationships, lead product introductions and tenders, and drive adoption of advanced technologies including robotics.

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 · High Wycombe

Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.

Johnson & Johnson MedTech · Breda, Netherlands · €68,600 – €119,600 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, supporting external research teams using clinical study data.

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 · Zug, Switzerland

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Johnson & Johnson MedTech · Horsham, United States · US$117,000 – US$201,250 pa

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrixed regulatory affairs team.