About Orthopaedics. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness. Learn more at We are searching for the best talent to join our Orthopaedics team as a Senior Robotics Verification & Validation (V&V) Engineer to be located in Raynham, MA or Boston, MA. Purpose:The Senior Robotics Verification & Validation (V&V) Engineer is responsible for ensuring that robotic products meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. The Sr. Robotics V&V Engineer works cross functionally with systems, software, hardware, robotics, manufacturing, and quality teams to ensure design outputs are thoroughly verified and validated against user needs, intended use, system and subsystem requirements, and risk controls. This role requires strong technical depth, excellent collaboration skills, and the ability to operate effectively in a regulated, multidisciplinary environment. You will be responsible for:In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:Collaborate with systems engineering to ensure requirements clarity, testability, and traceability from user needs, system and sub-system requirements, through verification and validation. Define minimum testable requirements post-change (risk-based, essential performance, basic safety). Develop and execute comprehensive V&V strategies and master system test plans for complex medical devices, including system verification protocols and regression plans that ensure robust requirements coverage; this includes investigational, integration, reliability, and formal V&V testing. Prepare and deliver system-level V&V documentation, including summary reports and verification results. Reviewing and approving sub-system verification deliverables to ensure alignment with overall system requirements. Design, validate, and implement test methods, including manual and automated test setups, to ensure they are suitable for verifying product requirements, including repeatability, reproducibility. Oversee the maintenance of robotics test lab facilities, ensuring all equipment and infrastructure are properly calibrated, serviced, and compliant with company safety, quality, and procedural standards; proactively identify and resolve issues to support uninterrupted testing and development workflows. Ensure compliance with regulatory standards (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 60601, ISO 14971). Support design transfer and product launch activities including complaints investigations. Investigate and document non-conformances, deviations, and test failures, drive root cause analysis and corrective actions. Interface with regulatory, quality, and manufacturing teams to support audits and inspections. Responsible for communicating business-related issues or opportunities to next management level. Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable. For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable. Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. Performs other duties assigned as needed. Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams. Support project resource and schedule planning. Qualifications / Requirements:Experience and Education: Bachelor’s or master’s degree in biomedical engineering, Systems Engineering, Electrical Engineering, or related field . years of experience in V&V engineering within the medical device industry. Experience with Class II or Class III medical devices is preferred. Knowledge of embedded systems, firmware/software testing, or electromechanical systems is a plus. Knowledge, Skills, Abilities, Certifications/ Licenses and Affiliations:Strong understanding of systems engineering principles and product development lifecycle (e.g., V-model, waterfall, Agile). Experience with requirements management tools (e.g., DOORS, Jama, Polarion). Familiarity with test automation tools and scripting languages (e.g., Python, Lab. VIEW, MATLAB). Excellent technical writing and communication skills. Certification in CQE, CQA, or Six Sigma is a plus. Proficient in sample size calculation and statistical methods for analyzing data. Location and Travel Requirements:The required location for this position is Raynham, MA or Boston, MA In office expectations are a minimum of 3 days per week, up to 5 days per week depending on project demand. An estimate of travel up to 30% may be required both domestic and international.