Program Manager

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 tandemdiabetes.com

A DAY IN THE LIFE:

The Program Manager, Translations & Localization is responsible for leading global translation and localization programs supporting Tandem Diabetes’ product development, regulatory submissions, commercialization, and post‑market sustaining activities. This role manages complex, multi‑language initiatives across product labeling, software/UI, packaging, training, marketing, and digital content, ensuring accurate, timely, and compliant delivery for global markets. The Program Manager acts as a key cross‑functional facilitator, partnering with Global Labeling, Regulatory Affairs, Quality, R&D, Clinical, Marketing, Digital, Manufacturing, and external language service providers (LSPs). This position requires strong program management expertise, deep understanding of medical device quality systems, and the ability to manage multiple concurrent workstreams in a regulated environment.

WHAT YOU’LL DO

Program Leadership

Lead end‑to‑end translation and localization programs for IFUs, packaging, software/UI text, tutorials, videos, marketing and digital content.

• Define program scope, schedules, milestones, dependencies and risk management plans across multiple languages and regions.
• Align translation workflows with product development, regulatory, and commercialization timelines.
• Drive the creation and maintenance of translation assets, including translation memories, glossaries/do not translate lists and regional requirements.

Cross‑Functional Collaboration

• Serve as the central liaison among Global Labeling, Regulatory, Quality, R&D, Clinical, Marketing, Digital, Manufacturing and external vendors.
• Partner with program managers and technical teams to plan and prioritize translation deliverables.
• Facilitate cross‑functional reviews, approvals and issue escalation.
• Provide regular status updates, risk assessments and metrics to stakeholders and leadership.

Vendor & Execution Management

• Initiate translation requests, manage vendor quoting and oversee execution by approved LSPs.
• Monitor vendor performance, quality, timelines and deliverables; drive continuous improvement.
• Coordinate in‑country reviews and delivery of final assets.

Quality, Compliance & Documentation

• Ensure translated content meets internal quality standards and complies with QMS procedures, regulatory requirements and regional regulations.
• Review translated content for accuracy and completeness.
• Support verification, approvals and change documentation.
• Maintain working knowledge of design controls, medical device standards and localization processes.

Digital & Marketing Support

• Partner with Marketing and Digital teams to coordinate translations, glossary adherence, in‑country reviews and deployment of localized assets.
• Work with Digital teams to ensure correct upload and deployment of localized content on web platforms.

Continuous Improvement

• Lead and contribute to initiatives that enhance translation workflows, localization tools, vendor governance, content reuse and PMO best practices.
• Identify opportunities to streamline processes, reduce cycle time and improve quality.

WHAT YOU’LL NEED

• Bachelor’s degree in engineering or a related field, or equivalent experience.
• 5+ years managing translation or localization projects in FDA‑regulated or ISO 14971–certified industries (medical devices, life sciences, or similar).
• Proficiency in one or more languages besides English preferred.
• Experience supporting diabetes‑related products preferred.
• Ability to work effectively in a matrixed environment and influence across organizational levels.
• Demonstrated success leading cross‑functional initiatives and managing multiple concurrent workstream