GROW WITH US:
Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry.
STAY AWESOME:
Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com
A DAY IN THE LIFE:
The Manufacturing Engineering Intern supports the manufacturing engineering team in applying engineering principles, scientific methods, and problem-solving techniques to the manufacture of infusion sets and related technologies. This role provides hands-on exposure to manufacturing line support, process improvement, documentation, equipment troubleshooting, and validation activities. The intern will assist with engineering projects focused on process optimization, cost reduction, and continuous improvement while gaining experience in a regulated medical device manufacturing environment.
Manufacturing Engineering Interns at Tandem are also responsible for:
- Supports manufacturing engineers with day-to-day production line activities and technical problem-solving.
- Assists in creating, revising, and organizing engineering documentation, including work instructions, BOMs, work orders, test methods, and quality specifications.
- Participates in process improvement initiatives focused on reducing waste, improving efficiency, and optimizing line performance.
- Assists with troubleshooting of production equipment, tooling, fixtures, and manufacturing processes under engineering guidance.
- Supports tooling and fixture design activities, including concept development, documentation, and implementation.
- Participates in Kaizen events, Lean Manufacturing initiatives, and Six Sigma projects to improve process capability and reduce costs.
- Assists in collecting and analyzing manufacturing data to identify trends, process variation, and improvement opportunities.
- Develops working knowledge of mechanical drawings, specifications, and basic GD&T principles.
- Supports R&D and Design Engineering in prototype builds, pilot activities, and process transfer projects.
- Assists with development of production test plans, requirements, and specifications.
- Helps support prototype development planning and pilot manufacturing activities.
- Participates in failure investigations, root cause analysis, and corrective action activities with Manufacturing, Quality, and R&D teams.
- Exposure to tools such as Fishbone diagrams, DOE, PFMEA/FMECA, and 5-Why analysis.
- Learns and applies Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
- Ensures work is completed in compliance with company policies, safety procedures, and regulatory requirements.
- Performs other duties and special projects as assigned.
WHEN & WHERE YOU’LL WORK:
Onsite: This position is fully onsite and open to candidates located in San Diego, California. Equipment for the role will be provided and training will occur onsite.
Schedule: This position will work Monday - Friday from 8:00 AM - 5:00 PM PST.
WHAT YOU'LL NEED:
Knowledge, skills & abilities:
- Basic understanding of engineering principles and manufacturing processes.
- Strong analytical and problem-solving skills with a willingness to learn in a fast-paced environment.
- Excellent verbal and written communication skills.
- Strong organizational and time-management skills.
- Ability to work effectively both independently and within cross-functional teams.
- Detail-oriented with strong documentation habits.
- Proficient in Microsoft Office Suite.
- Exposure to SolidWorks, Minitab, CAD software, or data analysis tools is preferred.
- Ability to learn technical documentation systems, process controls, and quality systems.
- Interest in medical device manufacturing, process development, and continuous improvement.
- This role requires flexibility to support evolving business needs, including occasional travel to supplier, manufacturing, and company sites as required.
- Able to work effectively in a team environment.
- Experience with Microsoft Office products including Outlook, Word, Excel, and PowerPoint.
- Comfortable working in a collaborative team environment.
- Clear verbal and written communication skills appropriate for technical discussions.
Minimum certifications/education