112 jobs
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 Blackpool
Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.
Johnson & Johnson MedTech Wokingham €93,500 – €149,845 pa
Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Builds relationships with key opinion leaders, supports investigator-initiated studies, reviews promotional materials, and provides scientific and HEOR support to cross-functional teams. Requires frequent conference attendance and up to 50% travel.
Johnson & Johnson MedTech Machelen, Belgium €93,500 – €149,845 pa
Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Involves building KOL relationships, managing investigator-initiated studies, providing scientific and HEOR support, reviewing promotional materials, and representing the company at conferences. Requires close cross-functional work with Clinical, Regulatory, Marketing and Market Access teams.
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.
