Medical Technology Jobs in Exeter

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

Leads the Accelerando program management function, partnering with high-priority new product development teams to de-risk and accelerate clinical trial execution. Acts as a trusted advisor to Compound Development Teams, running critical path analysis, threat and opportunity assessments, and project planning in Planisware and MS Project. Also leads a team, drives best-practice adoption and benchmarking across a global matrix organisation.

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

Leads the Accelerando program management function, acting as a trusted advisor to Compound Development Teams to de-risk and accelerate priority drug development programs. Facilitates cross-functional project planning in Planisware, conducts critical path and threat/opportunity analyses, and drives best practices and process improvements across a global matrix organisation.

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 · 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 · Machelen, Belgium

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Directs business adoption activities including change impacts, communications, training, readiness, role mapping and sustainment, working with programme and value stream leaders to ensure the organization realizes intended value.

Johnson & Johnson MedTech · Wokingham

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Directs a Business Adoption team covering change impacts, communications, training, readiness, role mapping and sustainment, advising programme and business leaders on adoption risks and pace of change.

Johnson & Johnson MedTech · Zug, Switzerland

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems across MedTech supply chain. Accountable for change strategy, communications, training, readiness, role mapping and sustainment, working with programme and business leaders across regions and value streams.

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.

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

Leads regulatory medical writing for the Immunology therapeutic area, preparing and finalizing clinical documents and serving as lead writer or point of contact for assigned programs. Manages direct reports, sets objectives, mentors junior writers and oversees external contractors, while driving process improvements and cross-functional coordination.

Johnson & Johnson MedTech · Allschwil, Switzerland

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Acts as lead writer or point of contact for assigned programmes, planning and directing writing groups while coaching junior staff and managing direct reports. Involves cross-functional collaboration, regulatory guideline knowledge and departmental process improvement.