Medical Technology Jobs in Exeter

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.

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.

Johnson & Johnson MedTech · High Wycombe

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, and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.

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.

Johnson & Johnson MedTech · Issy-les-Moulineaux, France

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.

Johnson & Johnson MedTech · Beerse, Belgium

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

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 · 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 · 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 · 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 · Maidenhead

Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects covering content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves mentoring junior writers, overseeing external contractors, and driving departmental process improvements.

Johnson & Johnson MedTech · Beerse, Belgium · €79,800 – €137,770 pa

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports in medical writing.

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

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports including hiring and performance discussions.

Johnson & Johnson MedTech · Toronto, Canada · US$134,000 – US$184,000 pa

Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned programmes, planning and directing writing groups, mentoring junior writers and overseeing external contractors. Also manages direct reports, setting objectives and running performance and development discussions.