Principal Process Engineer Warehouse

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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.

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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 endtoend (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 largemolecule 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 crossfunctional partners and strategic equipment vendors

• Serve as the logistics Subject Matter Expert (SME) for largemolecule 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 startup 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 datadriven 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 Bachelors degree in Engineering required

• Masters 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 crossfunctional 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 EHSbydesign and construction safety

• Startup 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 problemsolving capability communication skills and decisionmaking ability in a fastpaced 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 largemolecule biotherapeutic drug product environments

• Experience supporting greenfield or brownfield GMP aseptic manufacturing facility startups 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.

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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 parents consent for the background check.

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 & 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 external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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