Process Engineer - NPI/LCM

• Job title Process Engineer - NPI/LCM
• Function Supply Chain Engineering
• Sub function Process Engineering
• Category Engineer, Process Engineering (ST4 - E24)
• Location Raritan / United States of America
• Date posted May 30 2025
• Requisition number R-012764
• Work pattern Hybrid Work

This job posting is anticipated to close on Jun 06 2025. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

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

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Raritan, New Jersey, United States of America

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 .

Ethicon, a member of the Johnson & Johnson Family of Companies, is recruiting for an Process Engineer, New Product Introductions/Life Cycle Management.

Job Description

The Engineer, New Product Introductions/Life Cycle Management will entail providing process engineering support, planning and conducting activities related to the development of new manufacturing processes including researching current and emerging technologies, evaluating process cost, quality, and capability alternatives, and performing process characterization and optimization using design of experiments, problem solving and decision making tools; providing technical expertise in troubleshooting, design, and construction of manufacturing processes, systems, and equipment; planning, coordinating, documenting, and implementing all qualification and validation activities of new or improved manufacturing processes equipment and processes; ensuring fulfillment of all regulatory, safety, industrial hygiene, and environmental requirements for implementation of new products, processes, and equipment.

KEY RESPONSIBILITIES:

• Perform qualifications and project engineering activities for a complete project or portions of major projects to implement, optimize, or transfer new or existing manufacturing processes and/or equipment.
• Assist in new and existing process and equipment design.
• Assist in new process characterization activities.
• Prepare oral and written technical and progress reports regarding projects.
• Complete statistical analysis of data for decision making.
• Write technical experimental protocols and completion reports.
• Preparation of strategies, protocols, data collection, data analysis and presentation, and completion reports.
• Execute Process Excellence projects, including Lean Six Sigma, of both new and existing processes.
• Development and improvement of existing processes and methods for control and troubleshooting of manufacturing technical problems.
• Manage short to medium scale capital projects.
• Independently performs project activities with general instruction.
• Create and participate in a work environment in which change is embraced and collaboration is the foundation of success.
• Responsible for communicating business related issues or opportunities to next management level.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

Qualifications:

Required

• Degree in Engineering.
• 2 years experience in medical device manufacturing or related fields.
• Excellent verbal and written communication skills.
• Excellent interpersonal skills, particularly in cross-functional environments.
• Excellent critical thinking and problem solving skills.
• Knowledge of Statistical and analytical problem-solving methodologies.
• Knowledge of Good Manufacturing Practices (GMPs) and Quality System Regulations (QSRs).
• Knowledge of 21CFR 820, 21 CFR 4 and ISO 13485/EN ISO 13485.
• Knowledge of Microsoft Office (Word, Excel, PowerPoint, and Outlook.

Preferred

• Experience with Minitab.
• Experience in leading and managing projects and milestones.
• Six Sigma Green Belt or Black Belt certification or equivalent.

Other

• Domestic/international travel of up to 25%

Johnson & Johnson is an Affirmative 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 against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com.