Technology Manager, Quality Systems, BA

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: Technology Product & Platform Management Job Sub Function: Technical Product Management Job Category: People Leader All Job Posting Locations: Raynham, Massachusetts, United States of America Job Description: DePuy Synthes is recruiting for a Technology Manager, Quality Systems, BA , located in Raynham, MA or West Chester, PA or New Brunswick, NJ or Palm Beach Gardens, FL or Warsaw, IN The Technology Manager, Quality Systems, BA leads the business analysis capability supporting DePuy Synthes enterprise quality systems within the Supply Chain Technology function, Quality sub-function. This role manages a team of individual contributors and/or supervisors and is accountable for effective performance management, capability building, and career development. The Manager develops tactical and operational plans for quality systems requirements delivery, serving as the primary bridge between Quality, Regulatory, and Manufacturing process owners and the technology teams that build and support validated quality platforms. The role leads requirements elicitation, process and system analysis, functional design, and user acceptance across complaint handling, CAPA, nonconformance, document management, training, and audit systems Key Responsibilities Develops tactical and operational plans to achieve quality systems business analysis goals, and communicates plans to managers, supervisors, and individual contributors. Directs requirements elicitation, analysis, and documentation across quality processes including complaint handling, CAPA, nonconformance, deviations, change control, document management, training, and audit management. Leads the product functional design process based on an intimate knowledge of quality system users, regulated processes, and platform capability. Prioritizes and maintains the backlog for assigned quality platforms, balancing the requirements of Quality process owners, Regulatory, Manufacturing, and Technology stakeholders. Oversees translation of business requirements into user stories, functional specifications, acceptance criteria, and traceability matrices suitable for a validated environment. Directs current-state and future-state process analysis, identifying gaps, inefficiencies, and automation opportunities across quality workflows. Governs solution design reviews to ensure proposed configurations meet business need , regulatory requirements, and platform architectural standards. Leads user acceptance testing strategy and execution, including test script authorship, defect triage, and go/no-go recommendation. Ensures requirements and design artifacts satisfy computer system validation, change control, and documentation obligations under GxP , 21 CFR Part 11, and data integrity (ALCOA+). Directs impact assessment and requirements definition for integrations between quality systems and ERP (SAP), PLM, manufacturing execution, and post-market surveillance platforms. Partners with Quality leadership to define process and system KPIs, and translates reporting needs into platform requirements. Assesses the quality systems implications of technology change — including platform migrations, ERP implementations, and separation/carve-out activity — and defines requirements ahead of cutover. Anticipates bottlenecks, provides escalation management, and builds consensus by understanding stakeholder requirements and constraints. Leads business readiness, training material development, and change management to support adoption of new and enhanced quality system capabilities. Qualifications Education Required: Bachelor's degree in Information Systems , Computer Science, Industr ial Engineering, Life Sciences, Quality, Business, or a related discipline. Preferred: Master's degree in Information Systems , Engineering, or Business Administration. Experience and Skills Required: Minimum 8 years of progressive experience in business analysis, systems analysis, or solution delivery for regulated business applications in a manufacturing or MedTech environment. Minimum 2 years of experience leading teams, with demonstrated ability to