About the role#
The Automation Engineering Co-op supports the site automation team in a biopharmaceutical manufacturing facility. You will work on the implementation, maintenance, validation, and improvement of manufacturing automation systems. This six-month assignment offers hands-on experience with industrial automation platforms, computerized system validation, and digital manufacturing technologies within a regulated environment.
What you'll do#
- Support automation engineers in maintaining and improving manufacturing automation systems.
- Assist with the development and execution of computerized system validation (CSV) documentation, such as test scripts and validation reports.
- Participate in Site Acceptance Testing (SAT) and system commissioning activities.
- Troubleshoot and resolve issues related to automation systems and integrations.
- Collect, report, and analyze data using automation and manufacturing platforms.
- Manage change activities and update documentation to meet GMP requirements.
- Create and maintain 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 and efficiency.
- Learn and apply industry standards including ISA-88, ISA-95, GAMP 5, and GMP regulations.
What you'll need#
- Currently pursuing a BS or MS degree in Mechanical Engineering, Biomedical Engineering, Chemistry, Chemical Engineering, Biology, Biochemistry, or a related technical field.
- Preferred fields of study include Information Management, IT, Computer Engineering, Management Information Systems, Computer Science, Software Engineering, Data Science, or Cybersecurity.
- Cumulative GPA of 2.8 or higher.
- Available to work full-time (40 hours per week).
- Reliable transportation to and from the site.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
- Strong analytical, organizational, and time management skills.
- Ability to work independently and within a team.
- Permanent authorization to work in the U.S. without the need for future sponsorship.
- Prior experience in a cGMP environment and a basic understanding of large molecule drug manufacturing processes are preferred.
- Demonstrated leadership or participation in campus programs and community service.
Location & details#
- Location: Wilson, North Carolina.
- Work modality: On-site.
- Employment type: Full-time.
- Duration: 6-month assignment.
About Johnson & Johnson
Johnson & Johnson is a public company based in New Brunswick, New Jersey. Founded in 1886, it operates within the hospitals and health care industry. The company focuses on medical devices, diagnostics, and pharmaceuticals. It employs over 133,000 people across its global offices.
How to get in at Johnson & Johnson
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