343 jobs for “Healthcare Software Engineer”
Medtronic Madrid, Spain €27,200 – €40,800 pa
Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations. Collaborates with service engineers, repair centres and logistics teams in a regulated MedTech environment, and contributes to process improvements and UAT activities.
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 Breda, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Hybrid role with up to 10% travel.
Johnson & Johnson MedTech Leiden, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, release management, UAT, integrations, end-user support and audits, and drives automation, analytics and GenAI improvements. Hybrid working with up to 10% international travel.
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 Breda, Netherlands 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 high-priority new product development programs. Facilitates cross-functional project planning, critical path analysis and risk mitigation using tools such as Planisware and MS Project, while driving best practices and leading a high-performing team.
Johnson & Johnson MedTech Maidenhead US$137,000 – US$235,750 pa
Leads the Accelerando program management initiative, partnering with high-priority new product development programs to de-risk and accelerate launches. Acts as a trusted advisor to Compound Development Teams, driving critical path analysis, risk mitigation, and best-practice implementation using tools like Planisware and MS Project. Also leads a high-performing team and builds benchmarking networks across J&J and external partners.
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 Leeds
Leads the design and execution of professional education for the UK, building scalable learning pathways for healthcare professionals and governing onboarding, events, grants and cadaveric training. Manages a team and external partners including faculty and facilities, partnering with sales, marketing and compliance to close capability gaps and track programme effectiveness.
Johnson & Johnson MedTech Maidenhead
Shapes medical strategy for a portfolio of current and future oncology assets, leading integrated evidence generation, medical education and scientific engagement plans. Serves as a core member of the Cross-Functional Value Team, representing UK medical needs within EMEA and Global forums, and leads, coaches and develops a team of Medical Advisors. Provides medical signatory oversight and ensures compliance with the ABPI Code of Practice.
Johnson & Johnson MedTech New York, United States
Summer internship on a computer vision team, developing and evaluating AI/ML models for medical image and video understanding across modalities such as endoscopy, ultrasound, X-rays, dermatology, retinal OCT and histopathology. Involves building foundation and multimodal models, plus interviewing clinical staff to capture AI use cases and briefing reports.
Johnson & Johnson MedTech Spring House, United States
Summer internship on a computer vision team, developing and evaluating AI/ML models for medical image and video understanding across modalities such as endoscopy, ultrasound, X-ray, dermatology, retinal OCT and histopathology. Involves building foundation and multimodal models, plus interviewing clinical staff to capture AI use cases and briefing reports.
Johnson & Johnson MedTech New Brunswick, United States
Summer internship on a Computer Vision team, developing and evaluating AI/ML models for medical image and video understanding across modalities such as endoscopy, ultrasound, X-rays, dermatology, retinal OCT and histopathology. The role also involves interviewing clinical staff to capture AI use cases and building foundation and multimodal models that generalise across data types.
Johnson & Johnson MedTech Breda, Netherlands €68,600 – €119,600 pa
Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, supporting external research teams using clinical study data.
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.
