Staff Project Manager Advanced Technology

Job description

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: Robotics Job Category: Scientific/Technology All Job Posting Locations: Boston, Massachusetts, United States of America Job Description: We are seeking top talent for the Staff Project Manager Advanced Technology role on our DePuy Synthes Orthopaedics team. This position may be based in Boston, MA. 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 Orthopedics? Ready to join a team that’s reimagining how we heal? Our Orthopedics 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 https://www.jnj.com/medtech Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. Summary: The Staff Project Manager Advanced Technology is responsible for managing the advanced technology pre-charter funnel and for planning and executing assigned projects within the Advanced Technology group in Digital R&D, ensuring delivery against scope, schedule, cost, and quality in a regulated medical device environment. A primary focus of this role is to run the pre-charter intake process, prioritize and govern the funnel of advanced technology opportunities, track their progress and maturity, and ensure that projects are correctly managed and transferred into New Product Development (NPD) when they reach charter readiness. Reporting to the Platform Program Manager, this role owns the project-level integrated plan (WBS/IMS), project budget baseline and EVM tracking, project RAID management, change control, and stakeholder communications. The Project Manager coordinates cross-functional execution across software, systems, external partners, clinical and regulatory, and drives disciplined controls to enable predictable delivery outcomes. You will: Lead, mentor, and develop a team of design engineers, CAD designers/technicians, and documentation specialists (PLM) Design for Reliability (DfR) practices, including durability analysis, fatigue assessment, wear modeling, and lifetime testing strategies. Design for Manufacturability and Assembly (DfM/DfA) efforts to ensure scalable, repeatable, and cost‑effective production. Own and drive mechanical system requirements, ensuring alignment with system‑level requirements, user needs, performance targets, and regulatory constraints Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams. Partner with manufacturing engineering to optimize component sourcing, assembly processes, tolerances, and inspection methods. Oversee and guide tolerance stack‑up analysis, ensuring precision requirements are met for functional performance. Ensure appropriate use of analytical and simulation tools (FEA, thermal, kinematic modeling) to support design decisions and risk mitigation. Maintain mechanical design documentation, calculations, and analysis outputs suitable for design reviews, audits, and regulatory submissions. Collaborate closely with electrical, system, and software teams to ensure seamless mechanical‑electrical‑firmware integration. Define and review mechanical design concepts, trade studies, and architecture decisions to balance performance, reliability, manufacturability, cost, and serviceability. Participate in and contribute to risk management activities, including DFMEA and system‑level hazard analysis. Ensure mechanical risk controls are correctly implemented, verified, and validated. Review test results, investigate failures, and drive corrective actions for mechanical issues identified during development, validation, or field use. Ensure mechanical designs comply with applicable regulatory and quality standards (e.g., FDA, ISO 13485, IEC 60601 standards, material compliance). Partner with quality and regulatory teams to support design controls, audits, and regulatory submissions. Ensure documentation, design outputs, and change management comply with quality system requirements. Lead, mentor, and develop a team of design engineers, CAD designers, and documentation specialists (PLM) fostering technical excellence, accountability, and collaboration. Assign work, set technical direction, conduct design reviews, and provide coaching to support professional growth. Plan and execute engineering deliverables in alignment with program schedules and business objectives. Prepare annual and multi-year budget and resource plans aligned with business strategy Drive continuous improvement of engineering processes, CAD tools, and best practices. Stay current with advancements in mechanisms/mechatronics, precision gearing, materials, and manufacturing methods. Encourage innovation while maintaining disciplined engineering rigor, reliability, and compliance. 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 Support project resource and schedule planning. Performs other duties assigned as needed Qualifications: Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field 5+ years of project management experience within regulated class II or class III and product development environments (medical device, robotics, advanced technology, or software-enabled products preferred) Experience with phase-gate execution and design controls documentation in a QMS environment Deep understanding of regulated medical device product development and phase-gate execution, including FDA 21 CFR 820.30 / ISO 13485 design controls. Experience managing complex, cross-functional programs across software, systems, and hardware, including integrated planning across requirements, architecture, V&V