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**Job Function: **
Project/Program Management Group
**Job Sub Function: **
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Raynham, Massachusetts, United States of America
Job Description:
We are searching for the best talent to join our DePuy Synthes Orthopaedics team as a **Staff Project Manager R&D Spine **based in Raynham, 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: **As the Staff Project Manager R&D Spine plays a critical role in enabling and executing high-quality medical device development within a structured, Gate‑based New Product Development (NPD) framework. As a senior individual contributor and subject matter expert, this role leads complex, high‑impact R&D projects across implants, instruments, and enabling technologies while ensuring compliance with applicable regulatory and quality requirements, including FDA, ISO 13485, and 21 CFR 820.This position is responsible for end‑to‑end project planning and execution, including development of integrated project plans, ownership of Gate readiness activities, and delivery of key project milestones. The Staff Project Manager proactively identifies risks, dependencies, and critical path activities and partners with cross‑functional teams to align mitigation strategies with project and organizational objectives. Operating within a highly matrixed and regulated environment, the Staff Project Manager collaborates closely with R&D, PMO, Quality, Regulatory, Supply Chain, Marketing, Finance, and other supporting functions to enable effective decision making and consistent execution. Through strong leadership and communication, this role supports application of development and governance best practices and contributes to the effectiveness of the R&D operating model. In addition, the Staff Project Manager mentors junior project managers and drives continuous improvement of project management capabilities, contributing to scalable, compliant, and predictable product development outcomes.
You will:
- Lead multiple high-impact, complex development projects simultaneously.
- Drive projects through the Gate-based NPD process, ensuring required deliverables, reviews, and milestones are achieved.
- Develop, maintain, and execute integrated project plans, including schedules, resource needs, and financial allocations.
- Lead and influence cross-functional teams to achieve project objectives and enable timely, data-driven decisions.
- Communicate project status, risks, and mitigation plans clearly and effectively to diverse stakeholder groups.
- Proactively identify, escalate, and resolve risks, issues, and bottlenecks affecting critical path activities.
- Serve as the primary point of coordination with internal partners (e.g., manufacturing, finance, purchasing, sterilization, packaging) to align execution and interdependencies.
- Ensure project execution complies with applicable regulatory requirements, quality standards, and company policies
- Track project performance and deliver regular, leadership-level updates to senior stakeholders.
- Foster a collaborative, inclusive, and accountability-driven team environment; support and mentor junior project managers as appropriate.
Required Qualifications:
- Bachelor's degree in Engineering, Business Administration, or a related field
- 6+ years of progressive project management experience delivering complex, cross-functional initiatives
- Experience working in a regulated industry, preferably medical devices or life sciences
- Demonstrated success managing multiple concurrent projects from initiation through completion, with accountability for scope, schedule, and outcomes
- Proven ability to lead and influence cross-functional teams within a matrixed organization
- Strong analytical and problem-solving skills, with the ability to assess risks, evaluate trade-offs, and drive effective resolution
- Highly organized and self‑directed, with demonstrated success working independently in fast‑paced, matrixed environments while managing competing priorities and stakeholder expectations
- Experience supporting or leading geographically distributed teams
- Proficiency with standard project management and productivity tools (e.g., MS Project, Excel, PowerPoint, Word, Outlook), with the ability to adapt quickly to new systems
Preferred Qualifications:
- Advanced technical or business degree.
- Project Management Professional (PMP) certification.
- Demonstrated experience coaching and mentoring project managers.
- Familiarity with project lifecycle management (PLM) systems within a structured development environment.
- Experience using SharePoint and Microsoft Teams to support project governance, collaboration, and reporting.
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_Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. _
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource
Required Skills:
Preferred Skills:
Agility Jumps, Collaborating, Communication, Continuous Improvement, Problem Solving, Process Improvements, Project Management Office (PMO), Project Reporting, Research and Development
The anticipated base pay range for this position is :
$109,000.00 - $174,800.00
Additional Description for Pay Transparency:
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)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
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