Project Mgr, Business Product & Dev

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 Med Tech, 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.

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Job Function:
Regulatory Affairs Group Job Sub Function:
Regulatory Affairs Job Category:
People Leader All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

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.

DePuy Synthes is recruiting for a Project Manager, Business Product & Development, located in Raynham, Massachusetts, United States, West Chester, PA, Warsaw, IN, Palm Beach Gardens or FL, or NJ. The Project Manager, Business Product & Development is responsible for planning, coordinating, and executing regulatory‑related business product and development initiatives. This role supports the delivery of compliant, scalable regulatory solutions by partnering across Regulatory Affairs, Quality, IT, and business teams.

The position plays an important role in enabling regulatory readiness, process improvement, and operational efficiency while supporting business priorities in a regulated Med Tech environment. The role will collaborate with both Regulatory Affairs and IT partners to translate business requirements into application functional specs in the development of innovative solutions. The project manager leads the design, development and launch of new features, capabilities, and enhancements within existing applications or in the development of new applications within the Regulatory Operations System team portfolio.

In this role will utilize Process Excellence tools and methodologies to standardize and streamline processes and partner closely with RA business unit and regional leaders and SMEs (Subject Matter Expert) to foster continued process improvement.

• Lead and manage regulatory business product and development projects from initiation through delivery, ensuring alignment with regulatory and business requirements.
• Develop and maintain project plans, timelines, milestones, and status reporting for assigned initiatives.
• Partner with Regulatory Affairs, Quality, IT, and business stakeholders to define requirements and deliver compliant solutions.
• Coordinate cross‑functional teams to ensure timely execution and resolution of risks and issues.
• Support implementation and deployment of regulatory business products, tools, or process enhancements.
• Monitor project performance and ensure adherence to internal policies, quality system requirements, and regulatory standards.
• Prepare project documentation,…