Senior Quality Systems Specialist

USA-Medtronic MiniMed, Inc 1017; Los Angeles (CA); Vor Ort; USD 110.000 - 165.000; Vollzeit

Zusammenfassung

MiniMed in Los Angeles is seeking a detail-oriented Senior QMS Specialist with a strong foundation in quality regulations to drive QMS improvements, ensure compliance, and partner with cross-functional teams across Manufacturing, CAPA, Supplier Quality, Audit and Regulatory Affairs.

You will review changes, support audits, and help advance product quality through data analysis and process enhancements, while communicating clearly across the organization.

Aufgaben

• Reviews and facilitates development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
• Provides expertise and guidance to co‑workers in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
• Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
• Supports audit and inspection preparation, resolution of audit and inspection findings through all stages of the audits.
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Jobbeschreibung

We anticipate the application window for this opening will close on - 3 Nov 2026.

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.

About the Role

We are looking for a detail-oriented, proactive professional with a strong foundation in quality regulations and standards, the ability to manage competing priorities, and the communication skills to engage effectively across all levels of the organization. The Senior QMS Specialist partners closely with cross-functional stakeholders — spanning Manufacturing, CAPA, Supplier Quality, Audit and Regulatory Affairs — to ensure alignment with quality system requirements and regulatory expectations.

A Day in the Life

Review and drive QMS changes to support product and process releases and updates, sourced from local and enterprise level. Use excellent verbal and written communication skills to communicate and collaborate. Build and maintain positive relationships across the organization with strong relationship skills and act as a quality partner to other groups. Coordinate with team members, manager and other stakeholders to support both day‑to‑day activities and long‑term goals. Contribute to QMS quality by identifying, collaborating, creating and/or completing process improvements changes. Support monthly and quarterly quality metric reviews (as well as others) by facilitation, communicate, review and recording. Use critical thinking and data analysis to identify outliers or concerns and act to resolve.

Responsibilities

• Reviews and facilitates development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.
• Provides expertise and guidance to co‑workers in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
• Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.
• Supports audit and inspection preparation, resolution of audit and inspection findings through all stages of the audits.
• Pre