Experienced NPI Engineer

Johnson & Johnson • Cherry Hill, NJ

1d

About The Position

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 Description: Experienced NPI Engineer (Supplier & Process Engineering) Job Summary The Experienced NPI Engineer drives manufacturing and supplier readiness for new product introductions. This role leads the development and optimization of processes, manages supplier qualification activities, and ensures robust design transfer into manufacturing. The ideal candidate is a technically strong, hands-on engineer with solid experience in NPI, Supplier Engineering, and Operations, capable of independently solving complex problems and influencing cross-functional teams.

Requirements

• Bachelor’s degree in Mechanical, Industrial, Electrical, Biomedical, or related engineering field.
• 3–5 years of experience in manufacturing, NPI, supplier engineering, or process engineering.
• Strong understanding of manufacturing processes, quality systems, and design transfer principles.
• Demonstrated ability to lead cross-functional activities and manage complex technical tasks.
• Strong analytical, problem-solving, and data-driven decision-making skills.
• Excellent communication, stakeholder management, and collaboration capabilities.

Nice To Haves

• Experience in regulated industries (medical devices highly preferred).
• Strong knowledge of DFX methodologies, PFMEA development, Six Sigma, and validation standards.
• Proficiency with CAD tools, statistical analysis software (e.g., Minitab), and DOE methods.
• Experience working with suppliers globally and managing external manufacturing readiness.
• Lean manufacturing or Six Sigma certification (Green Belt or higher).

Responsibilities

• Lead the development and optimization of manufacturing processes for internal and external components and assemblies.
• Own and develop PFMEA, process flows, validation strategies, and control plans.
• Conduct supplier capability assessments, readiness reviews, and drive corrective action plans where needed.
• Provide expert DFM/DFA/DFX guidance during design phases and influence engineering decisions through data-driven recommendations.
• Plan, execute, and document process validations (IQ/OQ/PQ), ensuring compliance and robust process performance.
• Manage PPAP deliverables and oversee supplier qualification to ensure production readiness.
• Collaborate with R&D, Supplier Engineering, Operations, and Quality to ensure a seamless and compliant design transfer.
• Lead investigations of supplier or process issues using advanced problem-solving methodologies (8D, DMAIC, DOE).
• Ensure all documentation complies with quality system requirements and supports audit readiness.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees