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 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 PMPST. Hours may vary depending on specific projects that the Manufacturing team is currently working on.

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 Solid Works, 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/educational level:

• Currently pursuing a B.S. degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, Industrial Engineering, or related technical field.
• High School Diploma or equivalent, required.
• Currently enrolled as a junior or senior in a Bachelor’s degree program in a related field.

Minimum experience:

• Prior internship, laboratory, academic project, or hands-on manufacturing experience preferred.
• Exposure to regulated environments such as FDA, GMP, or ISO is a plus.
• Experience with Lean Manufacturing, Six Sigma, DOE, or process improvement projects through coursework is preferred.

COMPENSATION:

The starting base pay range for this position is $30.00 - $41.00 per hour. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market.

Please note that is a temporary position. As a temporary employee you will be employed through a staff agency partner. Benefits during your temporary assignment may be provided by the staffing agency. Access to Tandem sponsored benefits is contingent upon conversion from temporary to regular full-time status. Conversion is determined based upon business need and job performance.

YOU SHOULD KNOW:

Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information.

Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders.

SPONSORSHIP:

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

WHY YOU’LL LOVE WORKING HERE:

At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers.

BE YOU, WITH US!

We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us.

Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone.

REFERRALS:

We love a good referral! If you know someone who would be a great fit for this position, please share!

APPLICATION DEADLINE:

The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.

Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.