Job Information
J&J Family of Companies Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Device Assembly and Packaging Equipment in Wilson, North Carolina
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 (https://www.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 Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Wilson, North Carolina, United States of America
Job Description:
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
Ready to lead at the forefront of innovation? Learn more and apply today!
As part of the Global Process Engineering team, the Sr. Princ. Process Engineer serves as the recognized technical authority and Subject Matter Expert for device assembly and packaging equipment. This role is accountable for end‑to‑end (E2E) process engineering ownership of device assembly and packaging equipment, from conceptual design, commissioning and qualification, and initial equipment start-up for commercial manufacturing.
Key Responsibilities:
Lead development and delivery of device assembly and packaging 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 aseptic device assembly and packaging 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 aseptic device assembly and packaging equipment, collaborating with cross‑functional partners and strategic equipment vendors
Serve as DAP 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, 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, aseptic processing technologies, 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:
Bachelor’s degree in Engineering required (Mechanical Engineering preferred)
Master’s degree or MBA preferred
Experience and Skills:
Required:
Minimum of 10 years device assembly and packaging process engineering and/or capital project execution experience within a large-molecule, biotherapeutic cGMP environment
Strong background in aseptic, large-molecule, biotherapeutic drug product device assembly and packaging principles
Experience leading device assembly and packaging process engineering activities across the full project lifecycle, preferably within capital project execution
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 DAP SME
Demonstrated strength in resolving complex technical and regulatory challenges impacting the equipment and facility design of device assembly and packaging equipment for large-molecule, biotherapeutic products
Significant experience with implementing serialization and aggregation for the packaging of large-molecule, biotherapeutic products
Solid understanding of:
cGMP requirements for aseptic device assembly and packaging
Serialization and aggregation processes for finished biotherapeutic drug products
EHS requirements, with emphasis on EHS‑by‑design and construction safety
Start‑up processes and Commissioning & Qualification (C&Q) of aseptic equipment
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 aseptic equipment and facility design
Preferred:
Demonstrated leadership of capital projects for aseptic large-molecule, biotherapeutic device assembly and packaging equipment in the $50–$100MM range
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 device assembly and packaging
Experience with combination products and associated regulatory expectations
Other:
- This position will be 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 .]
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 https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Agile Decision Making, Coaching, Consulting, Corrective and Preventive Action (CAPA), Crisis Management, Cross-Functional Collaboration, Disruptive Innovations, Emerging Technologies, Industrial Hygiene, Lean Supply Chain Management, Process Control, Process Engineering, Product Costing, Program Management, Project Schedule, Science, Technology, Engineering, and Math (STEM) Application, Tactical Planning, Technical Credibility, Technical Research