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Manager, Compliance Engineering

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Tandem Diabetes Care Inc.
Full Time position
Listed on 2026-08-15
Job specializations:
  • Engineering
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 141800 - 177300 USD Yearly USD 141800.00 177300.00 YEAR
Job Description & How to Apply Below
Location: California

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

A DAY IN THE LIFE:

We are seeking a Manager, Compliance Engineering to lead compliance testing activities for a portfolio of innovative medical devices. This role is responsible for developing and executing compliance test strategies, managing product certification efforts, and ensuring products meet applicable safety, EMC, wireless, and regulatory requirements. As a key technical leader, you will work closely with Engineering, Quality, Regulatory Affairs, and external test laboratories to guide products from development through certification and commercialization.

The ideal candidate combines strong technical expertise in medical device testing with the ability to lead teams, manage complex projects, and drive continuous improvement.

Responsibilities:
  • Lead compliance testing and certification activities for new products and product modifications.
  • Develop compliance test strategies, plans, schedules, and resource requirements for product development programs.
  • Oversee product testing related to safety, EMC, wireless, environmental, and other applicable regulatory requirements.
  • Manage relationships with external test laboratories, certification bodies, and consultants, ensuring quality, cost, and schedule objectives are achieved.
  • Review and approve test plans, protocols, reports, risk assessments, and certification documentation.
  • Partner with Engineering teams to identify compliance risks early and drive effective testing and mitigation strategies.
  • Support design reviews and risk management activities with a focus on product safety, performance, and regulatory compliance.
  • Monitor changes in regulatory requirements and industry standards, assess impacts, and implement testing strategies to maintain compliance.
  • Develop and improve compliance testing processes, tools, metrics, and best practices to increase efficiency and predictability.
  • Lead, mentor, and develop a team of compliance engineers and test professionals.
  • Manage departmental budgets and forecasting related to compliance testing, laboratory services, equipment, and resources.
  • Ensure all activities are conducted in accordance with company policies and applicable quality, regulatory, privacy, and safety requirements.
WHAT YOU’LL NEED:
  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering or related technical discipline, or equivalent combination of education and applicable job experience.
  • Advanced coursework, Master’s degree, or professional licensing in related field desirable.
  • 5-8+ years of experience leading compliance testing, product certification, or regulatory engineering activities within the medical device industry.
  • 5+ years of experience leading/supervising in a high volume, medical device, biotech, or pharmaceutical environment preferred.
  • Strong knowledge of medical device safety and regulatory standards, including FDA QSR/QMSR, ISO 14971, and IEC 60601 series requirements.
  • Experience managing external compliance testing laboratories and certification programs.
  • Knowledge of EMC, electrical safety, wireless, and software/firmware compliance requirements for connected medical devices.
  • Proven ability to lead technical teams and manage multiple compliance testing programs simultaneously.
  • Exp…
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