This job posting is anticipated to close on Sep 30 2026. 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 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 EngineeringJob Sub Function:
Automation EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Wilson, North Carolina, United States of AmericaJob 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
Learn more and apply to this exciting new role!
The Automation organization is a dedicated team of professionals with diverse technical expertise responsible for the implementation, validation, qualification, and lifecycle support of ISA-95 Level 1 and Level 2 manufacturing automation systems, applicable interfaces, and Level 3 recipe and manufacturing-system integration. The team ensures that automated systems are fit for intended use and comply with applicable regulatory requirements, company manufacturing standards, data-integrity expectations, and cybersecurity requirements throughout the system lifecycle.
Reporting to the Drug Product Manufacturing Lead within the Site Automation organization, the Automation Engineer, Drug Product – Aseptic Filling provides technical automation and controls engineering ownership for the assigned aseptic filling area. This is an automation engineering role with direct accountability for manufacturing control systems and automation delivery; Process Engineering is a key partner but is not the functional scope of this position.
The role is responsible for the design, implementation, qualification, start-up, support, troubleshooting, and lifecycle management of automation solutions for Drug Product aseptic filling operations and their interfaces to site manufacturing systems. The engineer will work closely with Manufacturing, Process Engineering, Quality, Computerized System Validation (CSV), OT Infrastructure, MES, Digital, equipment suppliers, OEM controls teams, and system integrators.
Key Responsibilities:
Serve as the area Automation Engineer for Drug Product aseptic filling and provide direct technical ownership of the automation/controls scope under the DP Manufacturing Lead.
Support end-to-end automation delivery from concept and detailed design through controls development, FAT/SAT, construction support, commissioning, qualification, start-up, handover, troubleshooting, and steady-state lifecycle support.
Provide technical oversight for automation solutions supporting aseptic filling/finish operations and associated highly automated Drug Product equipment, including applicable isolator or barrier technologies, machine controls, batch/sequence control, SCADA/HMI, industrial networks, robotics, and site-system interfaces.
Review and challenge OEM and system-integrator automation designs, software/configuration, functional and design specifications, control narratives, system architectures, interface definitions, alarms/interlocks, and test documentation to ensure alignment with site and global automation standards.
Develop, implement, review, and troubleshoot PLC/DCS/HMI/batch and machine-control changes within the assigned area; ensure software and configuration are maintainable, standardized, documented, and appropriately controlled.
Plan, support, and execute automation FAT/SAT, commissioning, qualification, and start-up activities; lead technical issue resolution and drive automation punch-list items to closure.
Travel domestically and internationally, as required, to supplier/OEM, system-integrator, and Johnson & Johnson affiliate sites for FAT, technical training, knowledge transfer, and automation readiness.
Support automation interfaces to MES, historian, recipe/data platforms, and other site systems; ensure reliable data flow, traceability, and system integration for Drug Product manufacturing operations.
Author, review, and execute automation-related validation and qualification documentation; support risk assessments, investigations, deviations, CAPA, change controls, and regulatory/internal inspections.
Apply sound automation engineering principles, cGMP requirements, GAMP 5 practices, data-integrity expectations, cybersecurity controls, and lifecycle-management standards throughout the system lifecycle.
Partner with Manufacturing and Process Engineering on process requirements while retaining technical ownership of the automation/controls solution. Translate approved process and equipment requirements into robust, testable automation functionality.
Coordinate technically with equipment vendors, OEM controls teams, system integrators, CSV, OT Infrastructure, MES, Digital, Quality, and other partners to deliver an integrated and supportable solution.
Support operational readiness through training, documentation, maintenance/support models, spare-parts considerations, disaster-recovery/business-continuity planning, and transfer of automation-system knowledge to the site organization.
Use automation performance data and operational experience to identify continuous-improvement opportunities in reliability, system performance, validation efficiency, and manufacturing support.
Qualifications
Education:
A minimum Bachelor's degree in Engineering, Computer Science, Science, or a related technical field; required
Experience and Skills:
Required:
Minimum of 6 years of progressive automation and controls engineering experience in pharmaceutical or biopharmaceutical manufacturing.
Direct technical ownership of automated manufacturing systems in a cGMP environment, with hands-on responsibility for automation/controls scope supporting manufacturing operations and/or capital projects.
Proven Drug Product automation experience supporting aseptic or sterile manufacturing, including automated filling, inspection, assembly, packaging, or related highly automated systems.
Hands-on experience with ISA-95 Level 1 and Level 2 automation systems, including PLC and/or DCS controls, SCADA/HMI, batch or sequence control, machine controls, industrial networks, communication protocols, OT infrastructure, and associated hardware and interfaces.
Experience developing, reviewing, implementing, and troubleshooting automation software, system configurations, and engineering deliverables, including functional/design specifications, control narratives, interface definitions, alarm and interlock requirements, and system architectures.
Proven automation project execution experience, including OEM and system integrator coordination, controls design reviews, FAT/SAT, commissioning, qualification, start-up support, troubleshooting, and automation change control.
Solid understanding of ISA-88 and ISA-95 standards and their application within regulated manufacturing environments.
Knowledge of cGMP and computerized system validation expectations, including GAMP 5, 21 CFR Part 11, EU GMP Annex 11, data integrity, and risk-based validation principles.
Experience integrating manufacturing automation with Level 3 systems such as MES, historian, recipe management, data platforms, and related business or quality systems.
Strong written and verbal communication skills with the ability to partner optimally across Automation, Manufacturing, Process Engineering, Quality, CSV, OT Infrastructure, Digital, OEM, system integrator, and project teams while maintaining clear ownership of automation/controls deliverables.
Ability and willingness to support project travel and on-site execution needs, including periodic international travel to supplier/OEM, system integrator, and Johnson & Johnson affiliate sites for training, FAT, automation testing, and related project activities.
Candidates whose experience is limited to process engineering, validation, manufacturing operations, or equipment engineering without direct hands-on automation/controls responsibility will not meet this requirement.
Preferred:
Direct automation engineering experience with aseptic filling/finish equipment and associated isolator or restricted-access barrier technologies.
Experience with batch/sequence control, machine controls, robotics, motion control, and integration of aseptic filling equipment with MES and historian platforms.
Experience delivering automation scope for a large pharmaceutical capital project from design through controls development, FAT/SAT, commissioning, qualification, start-up, and operational handover.
Hands-on experience with platforms such as Rockwell Automation, Siemens, Emerson DeltaV, OSI PI, Werum PAS-X, or comparable PLC, DCS, SCADA/HMI, historian, and MES technologies.
Experience with reliability engineering, automation lifecycle management, operational readiness, and maintenance/support strategy development.
Good understanding of Industry 4.0, Industrial Internet of Things, advanced analytics, and evolving digital capabilities used to transform biopharmaceutical manufacturing.
Experience working with multiple OEMs, engineering partners, automation vendors, and system integrators in a global or multi-site organization.
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 (> 25%) 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.
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:
Artificial Intelligence (AI), Controls Compliance, Critical Thinking, Industrial Robotics, Industry Analysis, Innovation, Lean Supply Chain Management, Machine Learning (ML), Management Systems Implementation, Organizing, Problem Solving, Project Management, Prototyping, Robotic Automation, Science, Technology, Engineering, and Math (STEM) Application, Smart Systems, Technologically Savvy