CoOp Automation Engineer

Johnson & Johnson; Wilson (NC); On-site; USD 28,000 - 36,000; Full time

Job summary

Johnson & Johnson in Wilson, NC is seeking a full-time Co-op in Automation Engineering to support the Site Automation organization at a state-of-the-art biopharmaceutical facility. You will gain hands-on experience with automation platforms, MES, CSV, and GMP processes while collaborating with Manufacturing, Quality, Engineering, Maintenance, and IT teams.

The role emphasizes reliability, efficiency, and digital transformation, with learning opportunities across DCS, MES, BAS, PLC/SCADA, data

Qualifications

• Pursuing BS or MS in a technical field with GPA 2.8+.
• Able to work full-time (40 hrs/week) at site.
• Interest in automation, CSV, GMP, and digital manufacturing.

Responsibilities

• Support automation engineers in maintaining and improving manufacturing automation systems.
• Assist with development and execution of CSV documentation, test scripts, and validation reports.
• Participate in Site Acceptance Testing and commissioning activities.
• Troubleshoot automation systems and integrations with cross-functional teams.
• Support data collection, reporting, and analysis using data platforms.
• Contribute to SOP creation and maintenance.

Skills

Analytical skills

Microsoft Office

Communication skills

Team collaboration

Education

BS or MS in Mechanical Engineering / related field

Tools

Excel

PowerPoint

Job 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:

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

Job Description:

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)

Position Summary

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.

Key Responsibilities

• 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.

Learning Opportunities

The co‑op may gain exposure to:

• 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

Qualifications

Education:

• 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.

Experience and Skills:

Required:

• 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.

Preferred:

• Basic understanding of large molecule drug manufacturing processes is a plus.
• Strong problem solving and communication skills.
• Demonstrated leadership and/or participation in campus programs and/or community service activities.
• Experience working in a cGMP environment is preferred.

Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long‑term status that does not require company sponsorship.

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 and 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, please email the Employee Health Support Center ([e-mail]) or contact AskGS to be directed to your accommodation resource.

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