Manufacturing Engineering Internship
About The Position
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. We are seeking a motivated and detail-oriented Summer Intern to support the Manufacturing Engineering team within a regulated medical device manufacturing environment. This role provides hands-on exposure to production processes, continuous improvement initiatives, and engineering documentation that directly support safe and effective medical devices. The intern will work closely with Manufacturing Engineers, Quality, Operations, and Supply Chain to support daily production activities and improvement projects. This is an excellent opportunity to gain practical experience in a highly regulated industry.
Requirements
- Currently pursuing a Bachelor’s degree in Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Manufacturing Engineering, or related field.
- Junior or Senior standing preferred.
- Basic understanding of manufacturing processes and engineering principles.
- Strong problem solving and analytical skills.
- Strong communication skills, both written and verbal.
- Ability to work independently and within cross functional teams.
- High level of attention to detail and organizational skills.
- Eagerness to learn in a regulated manufacturing environment.
- Must be able to work on-site in an R&D lab environment as required
Nice To Haves
- Familiarity with data analysis tools such as Excel or Minitab preferred.
- Exposure to Lean Manufacturing concepts is a plus.
Responsibilities
- Assist Manufacturing Engineers in supporting daily production operations.
- Help troubleshoot process issues on the manufacturing floor under supervision.
- Support line balancing, workflow analysis, and capacity improvement activities.
- Participate in root cause investigations for nonconformances and process deviations.
- Support continuous improvement initiatives focused on safety, quality, delivery, and cost.
- Assist in data collection, analysis, and reporting of manufacturing metrics.
- Contribute to Lean Manufacturing activities such as 5S, standard work, and waste reduction projects.
- Help develop and update process maps and work instructions.
- Assist with creation and revision of manufacturing documentation including work instructions, process validation protocols, and engineering change documentation.
- Support engineering change orders and document control activities.
- Ensure compliance with FDA regulations, ISO standards, and internal quality system requirements.
- Support equipment qualification and process validation activities under guidance.
- Assist in protocol execution, data collection, and report preparation.
- Participate in small scale engineering projects with defined scope and timeline.
- Work with Quality Engineering to support CAPA and nonconformance investigations.
- Collaborate with Production Supervisors and Operators to understand process challenges.
- Present project updates and final results to the Manufacturing Engineering team.
Benefits
- Exposure to medical device manufacturing under FDA and ISO regulations.
- Practical experience in process improvement and validation activities.
- Mentorship from experienced Manufacturing Engineers.
- Opportunity to contribute to meaningful projects that impact patient safety.
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What This Job Offers
Career Level
Intern
Number of Employees
501-1,000 employees
