Principal Process Engineer - Warehouse

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Learn more and apply to this exciting new role!

As part of the Global Process Engineering team, the Principal Engineer Process Engineer serves as the recognized technical authority and Subject Matter Expert for logistics. This role is accountable for end‑to‑end (E2E) process engineering ownership of the logistics design. The role is responsible for definition of warehouse equipment including warehouse type (conventional, ASRS, etc.) and material handling equipment including robotic movement, material flows, and collaboration with automation and inventory management teams.

Key Responsibilities:

• Lead development and delivery of the logistics area, including specifications and drawings (URS, data sheets, technical specifications, P&IDs, PFDs) supporting large‑molecule, aseptic biotherapeutic drug product operations
• Provide process system ownership and technical leadership for logistics equipment used in biotherapeutic drug product manufacturing
• Assess vendor competency and capabilities; review and influence bid documents; and maintain accountability for project development and execution, including system performance
• Lead detailed design and development of logistics equipment, collaborating with cross‑functional partners and strategic equipment vendors
• Serve as the logistics Subject Matter Expert (SME) for large‑molecule, aseptic drug product projects, interfacing with A&E firms, construction partners, and equipment suppliers
• Lead and support equipment FAT, SAT, commissioning, qualification, and commercial production line start‑up activities
• Resolve complex technical issues during C&Q and ensure system readiness for qualification and commercial operation
• Partner closely with Manufacturing, Facilities, MSAT, Quality, Procurement, E&PS, Automation, Inventory Management, Cold Chain, and EHS to align priorities and accelerate execution
• Ensure alignment across evolving business needs, applying strong stakeholder and partner management skills
• Maintain current knowledge of industry trends and biotherapeutic regulatory expectations
• Apply data‑driven insights and market intelligence to guide technical and strategic decisions
• Ensure full compliance with company policies, cGMPs, regulatory requirements, and customer specifications

Qualifications

Education:

• A minimum Bachelor’s degree in Engineering required
• Master’s degree or MBA preferred

Experience and Skills:

Required:

• Minimum of 10 years logistics process engineering and/or capital project execution experience within a large-molecule, biotherapeutic cGMP environment
• Strong experience driving floorplan design for warehouse, material transport corridors, and in-process storage areas through simulation modeling, process mapping, and time studies to maximize flow efficiency
• Proven ability to build and maintain strong partnerships with cross‑functional stakeholders
• Ability to lead and influence multicultural teams and remote collaborators
• Extensive interaction with external partners (A&E firms, construction teams, and equipment vendors) as a logistics process engineer
• Demonstrated strength in resolving complex technical and regulatory challenges impacting the equipment and facility design in logistics for large-molecule, biotherapeutic products

Solid understanding of:

• cGMP requirements for logistics of large-molecule biotherapeutic products
• EHS requirements, with emphasis on EHS‑by‑design and construction safety
• Start‑up processes and Commissioning & Qualification (C&Q) for a large-scale biotherapeutic logistics operation
• Engineering design principles for biotherapeutic drug product manufacturing
• Construction, procurement, project controls, and project scheduling
• Strong technical depth, problem‑solving capability, communication skills, and decision‑making ability in a fast‑paced environment
• Passion for driving innovation in equipment and facility design

Preferred:

• Deep process engineering expertise from conceptual design through C&Q to operational readiness in large‑molecule biotherapeutic drug product environments
• Experience supporting greenfield or brownfield GMP aseptic manufacturing facility start‑ups in the logistics area

Other:

This position is located in Wilson, North Carolina, and will require full time on-site support. However, the design of the facility will occur at an Engineering firm with frequent travel (> 75%) required until the project shifts to the plant site of Wilson, NC.

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.

If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.”