308 jobs
Johnson & Johnson MedTech Prague, Czech Republic
Combines rigorous biostatistics with modern AI to build validated, reusable statistical solutions for pharmaceutical research and manufacturing. Involves hands-on development with LLMs, RAG and agentic workflows, plus Python services, APIs and MCP integrations, ensuring statistical integrity, reproducibility and traceability in a regulated environment.
Johnson & Johnson MedTech Raritan, United States
Combines rigorous statistical thinking with modern AI to build trustworthy, validated statistical solutions for pharmaceutical research and manufacturing. Involves hands-on development with LLMs, RAG and agentic workflows, plus Python services, APIs and MCP connections to R and Python tools. Works at the intersection of biostatistics, AI and scientific software development in a regulated, validation-sensitive environment.
Johnson & Johnson MedTech Spring House, United States
Combines rigorous statistical thinking with modern AI to build trustworthy, validated statistical solutions for pharmaceutical research and manufacturing. Involves hands-on development with LLMs, RAG and agentic workflows, building Python services and connecting R and Python tools via APIs and MCP. Works at the intersection of biostatistics, AI and scientific software development in a regulated, validation-sensitive environment.
Johnson & Johnson MedTech Beerse, Belgium
Combines rigorous biostatistics with modern AI to build validated, reusable statistical solutions for pharmaceutical research and manufacturing. Involves hands-on Python development with LLMs, RAG and agentic workflows, plus designing end-to-end architectures and ensuring statistical integrity in regulated environments.
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 Raynham, United States US$122,000 – US$245,000 pa
Provides global strategic and operational leadership for environmental, health, safety and Process Safety Management programs, ensuring regulatory compliance and embedding risk-based safety practices into manufacturing operations. Partners with site leadership, engineering and operations on audits, investigations and corrective actions, and coaches leaders to strengthen safety culture across a regulated medtech business.
Johnson & Johnson MedTech Warsaw, United States US$122,000 – US$245,000 pa
Provides global strategic and operational leadership for environmental, health, safety and Process Safety Management programs, ensuring regulatory compliance and embedding risk-based safety practices into manufacturing. Partners with site leadership, engineering and operations on audits, investigations and corrective actions, and coaches leaders to strengthen safety culture across a highly regulated medtech environment.
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 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 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 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 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 Maidenhead
Supports Clinical Trial Management Solutions including CTMS, Site Payments and Access Provisioning, acting as liaison between business partners, IT and suppliers. Handles study build, system integrations, release management, user acceptance testing, end-user support and audits, while identifying automation, analytics and GenAI improvements. Requires deep clinical development and GCP knowledge.
Johnson & Johnson MedTech Zug, Switzerland
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.
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.
