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MiniMed

Develops automated insulin delivery systems

Senior Quality Management Systems Specialist

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeNorthridge, Los Angeles, CA, USAIn-person

About the Job

Requirements

  • Requires a baccalaureate degree and a minimum of seven years of relevant experience, or an advanced degree and a minimum of five years of relevant experience.
  • Requires experience with Quality Management Systems, including Change Management, Continuous Improvement, and CAPA.
  • Requires experience using Microsoft Office Suite, especially Word, Excel, and PowerPoint.

Responsibilities

  • Review and drive Quality Management System changes to support product and process releases and updates sourced locally and at the enterprise level.
  • Build and maintain positive relationships across the organization and act as a quality partner to other groups.
  • Coordinate with team members, the manager, and other stakeholders to support day-to-day activities and long-term goals.
  • Contribute to Quality Management System quality by identifying, collaborating on, creating, and completing process improvement changes.
  • Support monthly, quarterly, and other quality metric reviews through facilitation, communication, review, and recording.
  • Use critical thinking and data analysis to identify outliers or concerns and act to resolve them.
  • Review and facilitate the development and maintenance of quality programs, systems, processes, and procedures to ensure compliance with policies and that service performance and quality conform to established internal and external standards and guidelines.
  • Provide expertise and guidance to coworkers in interpreting policies, regulatory or governmental regulations, and internal regulations to assure compliance.
  • Work directly with operating entities to provide ongoing process analysis oversight, enforce requirements, and meet regulations.
  • Support audit and inspection preparation and resolution of findings through all stages of audits and inspections.
  • Prepare reports and necessary documentation and provide them to applicable internal and external stakeholders.
  • Lead or support compliance-related activities such as audit readiness, Corrective and Preventive Actions (CAPA), and process improvement.
  • Act as backup for software validation or other quality activities as needed.
  • Ensure quality assurance programs and policies are maintained and modified regularly.
  • Facilitate uniform standards worldwide and enable best-practice sharing to support the company's mission globally.

Desired Qualifications

  • Experience in the medical device industry with relevant regulatory and standards knowledge is strongly preferred.
  • Direct experience with audit backroom or front room roles, non-product computer system validation, regulations and standards assessment, translation coordination, or multi-site/Quality Management System entity coordination is welcomed.
  • Broad knowledge of project management or process improvement methodology may be beneficial.
  • Six Sigma, Kaizen, Project Management Professional (PMP), or other project management certification is a bonus.
  • Experience with Agile, TrackWise, Microsoft Teams, Microsoft Project, or Power BI software systems.

About the Company

MiniMed

Develops automated insulin delivery systems

MiniMed develops insulin delivery and automated insulin delivery systems, plus related sensors, pens, and software. Its products couple glucose sensors with pumps or smart pens to automatically adjust insulin or simplify dosing. It differentiates itself with an integrated ecosystem of devices and software and a large share of recurring revenue from sensors, consumables, software and services across more than 80 countries. Its goal is to be a leading global provider of insulin delivery and glucose monitoring solutions that help people with diabetes achieve better glycemic control.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Los Angeles, CA
Founded
1983

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