Senior Software Quality Engineer

MiniMed

• $97K — $165K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Science, or a Technical field with 4+ years of relevant experience, or an Advanced Degree with 2+ years in relevant areas.
  • Experience in Quality, Engineering, and/or Software Development, especially in regulated environments.
  • Familiarity with software development lifecycle processes specific to embedded firmware.
  • Knowledge of regulatory standards such as IEC 62304, 13485, 14971, and FDA QMSR is highly preferred.
  • Strong verbal and written communication skills.

Responsibilities

  • Participate in product risk management through software Failure Mode Effects Analysis (FMEA) and product hazard analysis.
  • Drive compliance with design controls, risk management, and change control processes as part of the R&D team.
  • Engage in technical and product design reviews, reviewing relevant documentation and testing reports.
  • Manage and prioritize software issues in collaboration with the R&D team.
  • Contribute to Quality Management System reviews to ensure alignment with US and international standards.
  • Ensure proper documentation and traceability of requirements is maintained throughout the development process.
  • Support corrective and preventive action (CAPA) initiatives and assist the post-market team as necessary.

Benefits

  • Health, dental, and vision insurance coverage.
  • Access to a Health Savings Account and Healthcare Flexible Spending Account.
  • Life insurance and long-term disability coverage.
  • 401(k) plan with company match and an Employee Stock Purchase Plan.
  • Paid time off, holiday pay, and participation in incentive plans.
Full Job Description
We anticipate the application window for this opening will close on - 9 Oct 2026

About the Role

The Senior Software Quality Engineer works as part of the core product team to collaboratively drive the software development activities for embedded firmware and lead the risk management assessment and Quality deliverables.

Candidate will work with the R&D team to drive quality into product development, including collaborating with Regulatory, R&D, Marketing, Medical Safety, and post-market Quality, and implement strategies that enable continuous improvement.

Responsibilities may include the following and other duties may be assigned.

Hybrid role based in Northridge, CA
  • Participate in product risk management activities including software Failure Mode Effects Analysis (FMEA) and product hazard analysis.
  • Drive quality compliance with R&D team, including design controls, risk management, and change control processes, and engaging as Quality core team member with cross functional team members.
  • Participate in technical and product design reviews. Review design input and output artifacts including requirements, design documents, code reviews, verification and validation reports.
  • Manage and triage software issues with R&D team
  • Participate and support Quality Management System reviews of Standard Operating Procedures which align with US and international standards
  • Ensure that all requirement traceability is met and documented appropriately
  • Strong verbal and written communication skills with an ability to effectively communicate at multiple hierarchical levels in the organization.
  • Support CAPAs as needed, and post-market team for FCAs or HRAs as needed
  • Support internal and external audits


Must Have: Minimum Requirements

To be considered for this role, please ensure the minimum requirements are evident on your resume.

  • Bachelor's degree in Engineering, Science or Technical field with 4+ years of relevant experience in Quality, Engineering and/or Software Development OR Advanced Degree in Engineering, Science or Technical field with 2+ years of relevant experience in Quality, Engineering and/or Software Development.


Nice To Have:

  • Understanding of software development life cycle processes as applied to embedded firmware within the regulated medical device industry, and be familiar with IEC 62304, 13485, 14971, and FDA QMSR.
  • Candidate must have strong verbal and written communication skills.


#BetterDaysStartNow

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

Benefits & Compensation

MiniMed offers a competitive salary and flexible benefits package

Salary ranges for U.S (excl. PR) locations (USD):118000.00

For roles located in California, Seattle WA, Washington DC, Boston MA, and New York City, the salary range is $97,000 - $165,000 USD.

Actual compensation may vary based on factors including experience, education, certifications, skills, market conditions, internal equity, and geographic location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

At MiniMed, we are committed to supporting the well-being and financial security of our employees. Regular employees working 20 or more hours per week are eligible for a robust benefits package, including health, dental, and vision insurance, as well as access to a Health Savings Account, Healthcare Flexible Spending Account, life insurance, long-term disability leave, and a dependent daycare spending account. In addition, all regular employees enjoy incentive plans, a 401(k) plan with company match, short-term disability coverage, paid time off and holidays, participation in our Employee Stock Purchase Plan, and access to our Employee Assistance Program. Eligible employees may also benefit from our Non-qualified Retirement Plan Supplement and Capital Accumulation Plan, subject to IRS minimum earnings requirements. Please note that "regular employees" refers to those who are not temporary staff, such as interns, and some benefits may not apply to employees in Puerto Rico.

For further details about our comprehensive benefits, we encourage you to visit the link below.

MiniMed Benefits Overview

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