Senior Product Management Engineer

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld 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.

Learn more at

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

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations:

Plymouth, Minnesota, United States of America



Job Description

Johnson & Johnson Sustainability Solution (Sterilmed) is seeking a Senior Product Management Engineer for our Plymouth, Minnesota location.

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.

Learn more

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.

About Sustainability Solution

The Johnson & Johnson Medical Devices Companies (JJMDC) are committed to helping health systems reduce expenses and decrease environmental impact while meeting or exceeding OEM medical device functional requirements. Offering reprocessed single-use devices manufactured by Sterilmed, Inc., a part of the Johnson & Johnson Family of Companies, is one way in which we fulfill this commitment.

As a leading provider of reprocessing services, in addition to reprocessing devices originally manufactured by members of the JJMDC, we also offer reprocessed products from the other original manufacturers, to provide customers with more options to meet their needs.

Are you passionate about reprocessing to reduce medical waste? Ready to join a team that’s reimagining how we reprocess medical devices? Our team will give you the chance to deliver reprocessing solutions to customers. Your contributions will help effectively reduce medical waste through reprocessing.

Your unique talents will help patients on their journey to wellness. Learn more at

Purpose

This role focuses on managing and leading cross functional teams to transfer New Reprocessed Medical Devices into production. The position partners closely with R&D, Quality, Technical Lifecycle Management and External Manufacturer to design reliable, repeatable processes and/or equipment to ensure high-quality production through data-driven analysis, validation, and troubleshooting.

The role also includes process development, root cause analysis, and continuous improvement of manufacturing processes, along with authoring and maintaining validation and documentation to support regulated environments.

Key Role Responsibilities

• Serve as project manager of a multifunctional team to drive new product development activities from production readiness to launch.
• Plans validation strategies and owner of Master Validation Plan for New Product Introduction.
• Proposes and determines new or improved technologies to enhance product quality, manufacturing cost efficiencies, personnel safety and regulatory compliance.
• Oversees timely completion of pilot operations consistent with new product production activities of the department.
• Work closely with research and development team to develop processes that are manufacturable for new product.
• Develops project scopes, budgets and schedules for assigned projects and develops engineering specifications and documentation for manufacturing equipment.
• Ensures equipment is qualified/validated and supports safety and environmental initiatives.
• Develop and validate test methods for reprocessing of assigned devices.
• Reviews and edits all engineering documentation related to assigned projects, such as technical reports, work instructions and validation.
• Familiar with all aspects of medical device product development, including design, verification and validation, FDA submission, and design transfer into manufacturing.
• Author, revise, train, and provide support for production work instructions.
• Responsible for communicating…