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

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 · 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.