Medical Technology Jobs in Exeter

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

Strategic lead for modernising the Clinical Risk Management digital and data landscape, defining direction, priorities, governance and investment cases for CRM-owned digital capabilities. Partners with CRM leadership, RDQ functions, technology organisations and external vendors, and chairs decision-making forums on demand, change, risk and data. Retains strategic accountability while a Manager handles day-to-day process optimisation and digital administration.

Johnson & Johnson MedTech · Beerse, Belgium

Strategic lead for modernising the Clinical Risk Management digital and data landscape, defining roadmap, governance, investment cases and value measures. Partners with CRM leadership, RDQ, technology and external vendors, while a Manager handles day-to-day process optimisation and digital administration.

Reed · Stroud · £58,000 – £63,000 pa

Lead packaging and labelling validation for medical devices, managing transportation testing, shelf-life studies and equipment validation projects. Review technical documentation, BOMs and labelling content, drive process improvements, and lead non-conformance and CAPA investigations. Act as key contact during internal, customer and regulatory audits, supporting regulatory submissions and mentoring junior team members.

Appcast Enterprise · Clonmel, Ireland

Supports manufacturing operations by optimising processes, monitoring equipment and resolving issues that cause non-conforming products or low yields. Works within a quality system environment, interfacing with quality and R&D teams to integrate new products and processes, and participates in validation activities. May lead project teams and mentor less experienced engineers.

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 · 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.

Johnson & Johnson MedTech · Machelen, Belgium · US$122,000 – US$212,750 pa

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems. Governs change strategy, communications, training, readiness and role mapping, advising programme and business leaders on adoption risks and pace of change across value streams and regions.

Johnson & Johnson MedTech · Raritan, United States · US$122,000 – US$212,750 pa

Leads organizational change management for a multi-year global SAP S/4HANA transformation, harmonizing 40+ ERP systems. Accountable for change strategy, governance, communications, training, readiness and sustainment across value streams and regions, advising senior leaders on adoption risks and pace of change.

Johnson & Johnson MedTech · Wokingham · US$122,000 – US$212,750 pa

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 and sustainment, working with programme and business leaders to drive adoption and value realization.