Medical Technology Jobs in Exeter

Johnson & Johnson MedTech · High Wycombe

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedural requirements. Supervises vendors handling data anonymization and synthetization, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data and leads cross-functional projects within a matrix organization.

Johnson & Johnson MedTech · Blackpool

Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.

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 · 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 · Raritan, United States · US$117,000 – US$201,250 pa

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 matrixed regulatory 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.

Johnson & Johnson MedTech · Titusville, 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, timelines and scientific integrity, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Johnson & Johnson MedTech · Toronto, Canada · CA$87,000 – CA$140,300 pa

Writes and coordinates clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs and briefing documents for oncology programmes. Leads cross-functional document planning and review meetings, sets timelines and strategies, and mentors junior writers while acting as lead writer on most compounds. Hybrid role with three days onsite weekly.

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.

Johnson & Johnson MedTech · Titusville, 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 evaluations. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with oversight of deliverables prepared by other team members.