353 jobs for “Healthcare”
Medtronic Milan, Italy
Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise agreements and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability and data integration. Remote with around 70% regional travel.
Medtronic Brussels, Brussels, Belgium €92,800 – €139,200 pa
Provides legal advice on privacy, data protection and responsible data use across EMEA, covering GDPR, UK GDPR and ePrivacy. Drafts and negotiates data processing and transfer agreements, supports risk and transfer impact assessments, and advises on digital health, AI and cross-border data flows. Sits in the Global Data & Privacy Legal function, partnering with IT, Security, HR, Clinical and R&D.
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 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 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.
Johnson & Johnson MedTech High Wycombe
Summer internship on Johnson & Johnson's Computer Vision team, developing state-of-the-art AI/ML methods for medical image and video understanding across modalities such as endoscopy, ultrasound, X-rays, dermatology, retinal OCT and histopathology. The role combines hands-on design and evaluation of computer vision and multimodal foundation models with cross-functional clinical interviews to identify AI use cases and communicate findings to diverse partners.
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 Coventry
Owns territory business plans and sales targets for electrophysiology products across West Midlands hospital accounts, driving catheter utilisation and capital sales to grow market share. Builds clinical and non-clinical customer relationships, manages tenders and local pricing, and executes EMEA marketing launches alongside regional sales and technical specialist colleagues.
Johnson & Johnson MedTech Beerse, Belgium €82,000 – €141,450 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 matrix team.
