Senior Robotics Verification & Validation (V&V) Engineering Manager

Senior Robotics Verification & Validation (V&V) Engineering Manager Locations: Raynham, MA; Boston, MA Job Function: R&D Product Development Job Sub Function: R&D Software/Systems Engineering Job Category: People Leader 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. 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. Job Description The Senior Robotics Verification & Validation (V&V) Engineering Manager 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 Senior Robotics V&V Engineering Manager leads a team of Verification & Validation and Integration Engineers, providing technical and people leadership to ensure robotic systems meet all subsystem and system level requirements throughout development and release. Working cross functionally with systems, software, hardware, clinical, robotics, manufacturing, and quality teams, the Senior Robotics V&V Engineering Manager ensures that design outputs are verified and validated against user needs, intended use, system and subsystem requirements, and risk controls. This role requires strong technical depth, excellent collaboration and leadership skills, and the ability to operate effectively in a regulated, multidisciplinary environment. Key Responsibilities Lead a team of Verification & Validation and Integration Engineers to ensure robotic systems meet all defined subsystem and system level requirements. Collaborate closely with systems engineering, hardware, and software teams to ensure requirements are clearly defined, testable, and fully traceable from user needs and system/subsystem requirements through verification and validation. Define minimum testable requirements following design or requirement changes, applying a risk based approach that considers essential performance and basic safety. Develop and execute comprehensive V&V strategies and master system test plans for complex medical devices, including system verification protocols and regression strategies to ensure robust requirements coverage. This includes oversight of investigation, integration, reliability, and formal verification and validation 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. Coordinate and manage engagement with external test facilities (e.g., NRTLs, EMC, and restricted materials laboratories) to ensure full regulatory compliance and adherence to internal company policies. 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. Communicate business-related issues or opportunities to next management level. Follow 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. Ensure personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. 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 Required Bachelor’s or master’s degree in biomedical engineering, Systems Engineering, Electrical Engineering, or related field. 7+ years of experience in V&V engineering within the medical device industry. 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). Preferred Experience with Class II or Class III medical devices is preferred. Knowledge of embedded systems, firmware/software testing, or electromechanical systems is a plus. Familiarity with test automation tools and scripting languages (e.g., Python, LabVIEW, 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. Pay & Benefits Base salary: $137,000.00 - $235,750.00 Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: Equal Opportunity We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Johnson & Johnson is an Affiramtive Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated based on disability. #J-18808-Ljbffr Dormont Manufacturing Co