244 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 Rungis, France
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Manages MIR responses within four days, produces performance statistics, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech GB019 Bessemer
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Provides expert clinical guidance to healthcare professionals, manages MIR responses within four days, and produces performance reports with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Oslo, Norway
Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of J&J products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative outcome analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Pratica di Mare, Italy
Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists healthcare professionals with post-operative outcome analysis. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.
Johnson & Johnson MedTech Copenhagen, Denmark
Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical results. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Stockholm, Sweden
Supports the Medical Affairs team for intraocular lenses, analysing surgical cases and calculations, managing medical information requests within four days, and helping clinicians optimise post-operative outcomes. Works closely with Product Safety, Marketing, R&D and Commercial on clinical performance reporting and new product introductions, with home-office working and up to 20% travel.
Johnson & Johnson MedTech Pomezia, Roma, Italy
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech London
Supports the Medical Affairs team with intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise product use. Provides clinical expert support to healthcare professionals on post-operative outcomes, new product introductions, demos and clinical studies, working closely with Product Safety, Marketing, R&D and Commercial. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Limerick, Ireland
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Collaborates with product safety, marketing, R&D and commercial teams, providing expert support to healthcare professionals and internal customers on new product introductions. Home-office based with up to 20% travel across EMEA.
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.
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 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 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.
