Engineering Internship (Process, Mechanical, Automation & IT) – Summer 2027
NNE
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- Location
- Clayton, NC
- Work style
- On-site
- Job type
- Full time, Internship
- Posted
- Oct 13
- 7 days ago
Career path
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About the company
NNE
Civil engineering · 1,001 to 5,000 employees
What you'll do
- Support process, mechanical, automation, and IT/OT projects through design, studies, data collection, analysis, evaluations, and engineering deliverables.
- Assist with troubleshooting, process improvement, Automation and Data solutions, validation, commissioning, testing, and qualification.
Key skills
problem-solving skillsAnalyticaldetail-orientedstrong communicatormanage multiple priorities
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Read the full posting here
About the job: As an intern, you will gain hands-on exposure to pharmaceutical manufacturing projects and learn how engineering teams collaborate to design, implement, optimize, and maintain systems that support a highly regulated production environment. You will work on meaningful projects, develop technical and professional skills, and build connections with experienced engineers and fellow interns.
Location & Eligibility
This internship is based onsite at the NNE office located within the Novo Nordisk campus in Clayton, North Carolina. Due to the nature of the program, candidates should reside within a reasonable commuting distance of the work location. Housing, relocation assistance, and travel stipends are not available for this internship.
How You'll Spend Your Days
Assist engineering teams with project tasks and ongoing improvement initiatives.Support process, mechanical, automation, and IT/OT projects across the facility.Participate in engineering design, studies, data collection, analysis, and technical evaluations.Assist with equipment assessments, field walks, system inspections, and troubleshooting activities.Support the development and review of engineering deliverables, drawings, specifications, and reports.Contribute to process improvement and cLEAN initiatives focused on efficiency, reliability, and compliance.Collaborate with cross-functional teams to solve technical challenges and support project execution.Assist in developing Automation and Data solutions per S88/S95 standard and FDA guideline.Participate in validation, commissioning, testing, and qualification activities where applicable.Attend project meetings, team workshops, and professional development sessions.Complete assigned training and learn about pharmaceutical manufacturing, engineering standards, and industry best practices. Who You Are
Curious and excited to apply classroom knowledge to real-world engineering challenges.Analytical and detail-oriented with strong problem-solving skills.Comfortable working independently while also collaborating with multidisciplinary teams.Adaptable and willing to learn new technologies, systems, and processes.Organized and able to manage multiple priorities effectively.A strong communicator who can present ideas and ask thoughtful questions.