Co-Op Automation Engineer

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 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:
Career Programs Job Sub Function:
Non-LDP Intern/Co-Op Job Category:
Career Program All Job Posting Locations:
Wilson, North Carolina, United States of America

Location:

Wilson, NC Department:
Automation / Execution Systems

Reports To:

Site Automation Lead or Automation Engineering Manager Position Type:
Full-Time Co-op (6-Month Assignment)

The Automation Engineering Co-op will support the Site Automation organization in the implementation, maintenance, validation, and continuous improvement of manufacturing automation systems within a state-of-the-art, green field, biopharmaceutical manufacturing facility. The co-op will gain hands‑on experience with industrial automation platforms, manufacturing execution systems, computerized systems validation, digital manufacturing technologies, and GMP-regulated processes. This role provides a unique opportunity to work alongside automation engineers, manufacturing, quality, engineering, and IT teams while contributing to projects that support reliable, compliant, and efficient production operations.

• Support automation engineers in maintaining and improving manufacturing automation systems.
• Assist with the development and execution of computerized system validation (CSV) documentation, including test scripts, traceability matrices, and validation reports.
• Participate in Site Acceptance Testing (SAT), and system commissioning activities.
• Assist with troubleshooting and resolving issues related to automation systems and system integrations.
• Support data collection, reporting, and analysis activities using automation and manufacturing data platforms.
• Participate in change management activities and documentation updates in accordance with GMP requirements.
• Assist in the creation and maintenance of technical documentation, standard operating procedures (SOPs), and work instructions.
• Collaborate with cross-functional teams including Manufacturing, Quality, Engineering, Maintenance, and IT.
• Support continuous improvement initiatives focused on reliability, efficiency, and digital transformation.
• Learn and apply industry standards including ISA-88, ISA-95, GAMP 5, and applicable GMP regulations.

• Emerson DeltaV Distributed Control System (DCS)
• PAS-X Manufacturing Execution Systems (MES)
• Honeywell Building Automation Systems (BAS)
• Siemens and Rockwell PLC and SCADA technologies
• OSI PI Historian and data analytics platforms
• Computerized System Validation (CSV)
• Large Molecule Drug Substances Pharmaceutical manufacturing processes
• Industrial automation networks and cybersecurity fundamentals
• Digital manufacturing and Industry 4.0 initiatives

Currently pursuing a BS or MS degree in Mechanical Engineering, Biomedical Engineering, Chemistry, Chemical Engineering, Biology, Biochemistry, or a related technical field. Preferred fields include Information Management, Information Technology, Computer Engineering, Management Information Systems, Computer Science, Software Engineering / Development, Data Science, Cybersecurity. Have a cumulative GPA of 2.8 or higher, which is reflective of all college coursework.

• Available to work full-time (40 hrs./week) with reliable transportation to and from site
• Strong analytical skills and attention to detail.
• Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
• Excellent organizational and time management skills.
• Strong verbal and written communication skills.
• Ability to work independently and as part of a team.
• Basic understanding of large molecule drug manufacturing processes is a plus.
• Strong problem solving and communication skills.
• Demonstrated leadership…