Internship – Engineering – Sustaining / Process Engineering

Biomerics•Salt Lake City, UT

About The Position

Biomerics Engineering Interns will become part of a Sustaining and Process Engineering team, reporting to a Senior Engineer or Engineering Manager. This internship focuses on supporting released medical device products and manufacturing processes, driving continuous improvement, and ensuring stable, capable, and compliant production in a regulated environment. The intern will work closely with manufacturing, quality, supply chain, and engineering teams to support day-to-day operations, troubleshoot issues, and implement process improvements across existing products.

Requirements

Currently pursuing an Engineering degree and at least a Junior in the program.
Create models and drawings using CAD, preferably SolidWorks
Strong attention to detail to support work in a regulated medical device environment.
Ability to analyze problems, think independently, and execute assigned tasks with minimal supervision.
Excellent verbal and written communication skills.
Strong interpersonal skills and ability to work effectively in a cross-functional, team-oriented environment.
Willingness to learn, accept feedback, and continuously improve.
Flexibility to adapt to changing priorities in a dynamic manufacturing environment.
Proficiency with Microsoft Word and Excel.

Nice To Haves

Engineering or technical disciplines such as:
Mechanical Engineering
Manufacturing Engineering
Electrical Engineering
Industrial Engineering

Responsibilities

Support process engineering activities for released products, including manufacturing support, issue resolution, and process optimization.
Assist in the improvement and documentation of manufacturing, assembly, and test processes.
Participate in continuous improvement initiatives focused on yield improvement, scrap reduction, cycle time reduction, and cost optimization.
Support process troubleshooting and root cause investigations (e.g., nonconformances, deviations, CAPAs) under guidance of senior engineers.
Contribute to the design, modification, and qualification of tooling, fixtures, and manufacturing equipment for existing products.
Assist with process validation activities (IQ/OQ/PQ), including data collection, analysis, and report generation.
Support design changes and engineering change orders (ECOs) for released products.
Assist with the creation and maintenance of Standard Operating Procedures (SOPs), work instructions, and manufacturing documentation.
Collaborate with manufacturing operators, quality, and suppliers to ensure robust and repeatable processes.
Gain hands-on experience working in an ISO 13485–regulated medical device manufacturing environment.