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 type 1 diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at https://www.tandemdiabetes.com/

 

WHEN & WHERE YOU’LL WORK: 

On-Site: This role is on-site five days a week at our Headquarters in Del Mar due to the nature of the work involved.

A DAY IN THE LIFE:

A Senior Mechanical Engineer at Tandem Diabetes Care is a senior team member contributing to the design, troubleshooting, documentation, and testing of mechanical systems for the Company’s medical devices. This individual works with mechanical, electrical, and software engineers, as well as the Manufacturing and Operations teams to contribute to the determination of hardware requirements and/or influences on hardware design.

A Senior Mechanical Engineer at Tandem also:

Participates in the research and development of mechanical components and systems for the Company’s medical device(s), utilizing advanced knowledge of mechanical theory and materials properties. Contributes to planning, design, analysis, and optimization of mechanical parts, components, moving mechanisms, precision assemblies, mechanical systems, equipment and packaging, or optical systems. Participates in determining design approaches, parameters, and requirements. Prototypes and iterates designs based on user needs and feedback for mechanical systems and specialized computer-controlled equipment. Materials selection for intended use, biocompatibility, sterilization compatibility, and durability (e.g., metals, polymers, ceramics, etc.). Defines appropriate feature tolerances and conducts tolerance analysis for components and assemblies. Documents the analysis and presents results and conclusions. Selects components and equipment based on analysis of specifications and reliability. Ensures device performance under real-world conditions with design verification, including mechanical testing and reliability analysis. Embraces the Design Control process by participating in design reviews and maintaining documentation for design history files. Collaboration with regulatory teams to ensure designs meet FDA/ISO requirements for safety and performance. Analyzes equipment to establish operating data, conducts experimental tests and evaluates results. Contributes to the review of vendor capability to support development. Confirms completion of required training plan before assuming job responsibilities. Ensures work is performed in compliance with company policies including Privacy/HIPAA and other regulatory, legal, and safety requirements. Supports other departments as needed and considers project-wide impacts in decision making.

 

WHAT YOU’LL NEED:

Working knowledge of federal and other regulations, e.g., QSRs and ISO 13485 and 14971. Knowledge of Good Documentation Practices (GDP). Experience with Design for Manufacturability and integration experience in a manufacturing environment, to assist with the transfer of process fixtures and testing methodology to manufacturing. Experience with Solid Works/PDM/PLM and simulation software. Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information. Skilled at promoting team cooperation and a commitment to team success. Adept at seeing change as an opportunity to improve business performance and campaigning for it when necessary. Competent with MS Office and Internet. Bachelor’s degree in Mechanical Engineering, Biomedical Engineering or related field or equivalent combination of education and applicable job experience. 5 years of experience in the field including detailed design, design testing and documentation, and prototype fabrication of biomedical devices, including experience with all stages of development from conceptual design to market release. Experience with Good Design Practices. Integration experience in a manufacturing environment, to assist with the transfer of process fixtures and testing methodology to manufacturing.

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 are firmly committed to being an equal opportunity employer and maintaining a diverse and inclusive environment. We value and embrace that every single one of us brings value 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.

COMPENSATION & BENEFITS:

The starting base pay range for this position is $96,000 to $120,000 annually. 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. In addition to base pay, Tandem offers a competitive compensation package that includes bonus, equity, and a robust benefits package.

Tandem offers health care benefits such as medical, dental, vision available your first day, as well as health savings accounts and flexible saving accounts.  You’ll also receive 11 paid holidays per year, a minimum of 20 days of paid time off (with accrual starting on day 1) and you will have access to a 401k plan with company match as well as an Employee Stock Purchase plan.  Learn more about Tandem’s benefits here!

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.

REFERRALS:

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

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.

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.

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