M

MiniMed

Develops automated insulin delivery systems

Senior Software Quality Engineer

Biomedical Engineering & Medical DevicesUpdated on Nov 13
Full-time

About the Job

Requirements

  • Bachelor’s degree in Engineering, Science, or a Technical field with at least 4 years of relevant experience in Quality, Engineering, and/or Software Development, or an Advanced Degree in Engineering, Science, or a Technical field with at least 2 years of relevant experience in Quality, Engineering, and/or Software Development.
  • Understanding of software development life cycle processes as applied to embedded firmware within the regulated medical device industry, and familiarity with IEC 62304, 13485, 14971, and FDA QMSR is preferred.
  • Strong verbal and written communication skills are required, with the ability to communicate effectively at multiple hierarchical levels in the organization.

Responsibilities

  • Participate in product risk management activities, including software Failure Mode and Effects Analysis (FMEA) and product hazard analysis.
  • Drive quality compliance with the Research and Development team, including design controls, risk management, and change control processes, and engage as a Quality core team member with cross-functional team members.
  • Participate in technical and product design reviews, and review design input and output artifacts, including requirements, design documents, code reviews, and verification and validation reports.
  • Manage and triage software issues with the Research and Development team.
  • Participate in and support Quality Management System reviews of Standard Operating Procedures that align with U.S. and international standards.
  • Ensure that all requirements traceability is met and documented appropriately.
  • Support Corrective and Preventive Actions (CAPAs) as needed, and support the post-market team for Field Corrective Actions (FCAs) or Health Risk Assessments (HRAs) as needed.
  • Support internal and external audits.

Desired Qualifications

  • Understanding of software development life cycle processes as applied to embedded firmware within the regulated medical device industry, and familiarity with IEC 62304, 13485, 14971, and FDA QMSR.

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

Recently Posted Jobs

Explore more opportunities at MiniMed

See more jobs