New · posted Oct 15
Tandem Diabetes Care · Medical Devices
Sr. Supplier Quality Engineer I
- San Diego, CA
- Hybrid
- Full-time
- Senior & Principal
Open until filled
The role
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
EXTRA AWESOME
- Bachelor’s degree in Engineering, preferably Electro-Mechanical Engineering or the equivalent education and applicable work experience.
- ISO lead auditor, Certified Quality Engineer, or equivalent preferred.
- Minimum 5 years’ related experience in Supplier Quality or related engineering positions
- Familiarity in the production of PCB, PCBA, electro-mechanical assemblies and plastic molding is highly desirable.
- Medical device manufacturing or FDA-regulated industry experience, highly preferred.
- Supplier or lead quality auditing experience in a regulated company, highly preferred.
- Experience in managing 3rd party contract manufacturers is a plus.
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.
We love a good referral! If you know someone who would be a great fit for this position, please share!
What you need
- Direct experience with suppliers and contract manufacturers who produce components or assembly parts in a regulatory environment.
- Proficient knowledge of Quality Engineering policies, principles and best practices including quality standards: ISO 13485, ISO 14971, ISO 9001 and other appropriate industry standards.
- Competent in QMS Audit and Process Audit practices with ability to readily recognize non-conformances.
- Must be able to explain audit results and influence other's understandings of audit observations in a culturally sensitive, tactful, and professional manner.
- Strong knowledge and application of principles outlined in Good Manufacturing Processes (GMP).
- Strong knowledge of and demonstrated experience using statistical techniques: sampling theory, probability, capability, and SPC.
- Strong knowledge of and demonstrated experience using problem solving methodologies: 5-why analysis, fault tree analysis, cause and effect diagram etc.
- Ability to work independently to identify potential quality issues and implement solutions.
- Understanding of mechanical drawings & specifications including geometric dimensioning and tolerances (GD&T).
- Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information.
What you'll do
The Sr. Supplier Quality Engineer I is responsible for conducting and overseeing supplier audits, qualifying new suppliers, and monitoring the performance of current suppliers. An experienced team member providing quality guidance and support for supplier management activities such as qualifications, change notifications, audits, evaluations and performance to assure conformance to established standards, specifications and risk reduction. Acts as an instrumental member of the team to optimize and continuously improve supplier operations to meet department, business unit and company objectives. Provides suggestions, guidance and feedback to suppliers to ensure quality materials and components are delivered for use in Tandem’s product operations.
The Sr. Supplier Quality Engineer I are also responsible for:
- Manage, lead and/or oversee supplier audits to meet company, quality, and regulatory requirements, including country-specific requirements for the suppliers; responsibilities extend to audits performed by 3rd party contractors.
- Generate, approve, review and monitor Supplier CAPA plans and activities to investigation and closure, including objective evidence of verification of effectiveness.
- Partner with Quality, process owners, legal and suppliers to create and revise Quality Agreements, as needed.
- Qualify, manage, and monitor supplier performance per Tandem supplier management approved processes. Identify gaps in current processes to develop, define, establish, and document new processes, as needed.
- Demonstrated ability to lead, develop, communicate & implement strategies for continuous improvement and development of existing or new suppliers and contract manufacturer.
- Ability to build relationships and work with suppliers or contract manufacturer to establish and maintain controlled consistent manufacturing processes and methods suitable to the nature of the components or assembly parts they supply.
- Independently leads and completes supplier activities such as supplier evaluations, change notifications, and validations.
- Facilitates quality oversite of Tandem’s 3rd party contract manufacturers.
- Ability to provide guidance to suppliers or contract manufacturer for quality engineering disciplines and statistics such as but not limited to PFMECA, DMAIC, Lean, Problem-Solving tools, capability analysis, DOE, IQ/OQ/PQ validations.
- Responsible for reporting quality trends and information to management on the performance of suppliers or contract manufacturers.
- Follows up with suppliers for component related non-conformances identified during Tandem’s incoming inspection, in-process inspection, final test, quality complaints, and as applicable product returns.
Pay and benefits
$100,000 – $123,000 a year
Employer providedThe starting base pay range for this position is $100,000 - $123,000 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 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!
Medical, dental, vision from day one
HSA and FSA
11 paid holidays
20+ days PTO
401k with company match
Employee Stock Purchase Plan
Where you'll work
San Diego, CAHybridOpen in Maps (opens in a new tab)
More jobs in San Diego, CAWorking conditions
WHEN & WHERE YOU’LL WORK
Hybrid: This role will be a mix of in-office work at our Barnes Canyon facility in San Diego, CA and remote work. This position is expected to be in office 2 days per week but may vary depending on business demands.
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.
From the posting
About Tandem Diabetes Care
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.
Equal opportunity, accessibility and legal noticesTandem Diabetes Care's statements, word for word
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.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 9% below the US median for Quality Assurance roles at this level.
This roleEmployer provided
Senior & Principal roles in California84 roles publishing pay
Senior & Principal roles in the US284 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $100,000 | — | $123,000 |
| California (middle half) | $118,625 | $135,000 | $158,625 |
| All US (middle half) | $103,375 | $122,750 | $137,500 |
This role: Tandem Diabetes Care's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Tandem Diabetes Care's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk17
- GMP and compliance9
- Collaboration and leadership9
- Lab testing and methods5
- Investigations and CAPA3
- Validation and qualification3
- Documentation and SOPs2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
Company hiring pulse
Tandem Diabetes Care on Regulatory Jobs
- 4
- Open roles
- 4
- Distinct roles
- 3
- Locations
By discipline
- Quality4 100%
By level
- Senior & Principal3 75%
- Associate & Specialist1 25%
More roles at Tandem Diabetes Care
- View role
Sr. Quality Engineer - Manufacturing
CaliforniaSenior & PrincipalMedical Devices$110K–$121K
- View role
Quality Assurance Associate II (Temp to Hire)
San Diego, CAAssociate & SpecialistMedical Devices$47K–$50K
- View role
Quality Control Inspector II
Irvine, CASenior & PrincipalMedical Devices$56K–$62K
Similar Quality Assurance roles elsewhere
- View role
Senior Supplier Quality Engineer
iRhythmOrange County, CA · HybridSenior & PrincipalMedical Devices$99K–$129K
- View role
Senior Design Quality Engineer
iRhythmSan Francisco, CA +1 more · HybridSenior & PrincipalMedical Devices$138K–$180K
- View role
Staff Quality Engineer, New Product Introduction
StrykerIrvine, CASenior & PrincipalMedical Devices$103K–$171K
- View role
Senior Quality Engineer, New Product Introduction
StrykerIrvine, CASenior & PrincipalMedical Devices$89K–$149K
Sr. Supplier Quality Engineer I at Tandem Diabetes Care
Open until filled. $100K–$123K a year, employer provided.