Sr. Mgr R&D Applications & Master data
Johnson & Johnson
- Location
- Raynham Massachusetts United States of America
- Work model
- On-Site
- Level
- Senior
- H-1B history
- 2 approvals (FY2023)
- Posted
- Aug 18, 2026
Skills
About this role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: R&D Product Development Job Sub Function: Multi-Family R&D Product Development Job Category: People Leader All Job Posting Locations: Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America Job Description: DePuy Synthes is recruiting for a Sr. M g r , R&D Applications & Master Data , located in Raynham, Massachusetts . Senior Manager , R&D Applications & Systems DePuy Synthes is seeking a Senior Manager to lead the global R&D Applications & Systems team. In this role you will define the Product Lifecycle Management (PLM) product and platform strategy that enables R&D and product development across the enterprise. This role will own enterprise-scale PLM capabilities and integrations across R&D, Quality, Regulatory, Manufacturing, and Supply Chain. As Business Product Manager for PLM, ALM, and CAD capabilities — including an Agile → Windchill transformation — you will enable trusted, traceable R&D applications and master data that accelerate innovation, support regulatory compliance, and shorten time-to-market for medical devices.
Key responsibilities
Product strategy & governance Define and execute the global PLM/ALM/CAD product and platform strategy aligned to R&D and enterprise IT objectives. Own product-side governance, roadmap, and budget accountability for R&D applications and master data domains where R&D is the primary business owner. Maintain a harmonized R&D application catalog and technical stack to reduce fragmentation while preserving specialized engineering capabilities. Business Product Management & delivery Serve as the Directly Responsible Individual (DRI) and Business Product Manager for PLM development and deployment initiatives, including an Agile → Windchill transformation. Own backlog prioritization, feature decomposition, release planning, and acceptance of delivered value. Participate in PI Planning and Agile ceremonies as required. Define and track outcomes and KPIs (adoption, lead time, data quality, delivery performance) and use data to drive decisions and course corrections. Master data strategy & integrations Define and operationalize master data models, governance, stewardship, and quality practices for critical R&D domains. Establish data quality management (profiling, validation rules, remediation workflows) and root-cause analysis for recurring data defects. Partner with enterprise architecture and IT to design and govern integrations that ensure data lineage and end-to-end traceability between PLM, Quality, Regulatory, ERP, Manufacturing, and analytics systems. Team, vendor & stakeholder leadership Lead, develop, and scale a team that partners with R&D stakeholders to capture business needs, translate them into technical requirements, and prioritize work with IT and external vendors. Manage vendor selection, third-party relationships, contracts, and vendor delivery performance. Collaborate with IT, cybersecurity, Quality, and Regulatory partners to ensure solutions meet compliance and validation requirements (FDA, ISO 13485, EU