Staff Cloud Software Quality & Compliance Engineer

Posted 3 Days Ago
5 Locations
In-Office or Remote
103K-222K Annually
Mid level
Healthtech
The Role
Guide software teams in quality management systems, lifecycle governance, risk management, audit readiness, and compliance for cloud-based and connected products. Develop quality procedures, support design and release reviews, maintain audit evidence, conduct gap assessments, and assist with investigations and corrective actions. Partner with engineering, security, privacy, regulatory, IT, and operations teams to improve compliant software delivery across Agile, DevOps, and CI/CD environments.
Summary Generated by Built In
Work Flexibility: Remote or Hybrid or Onsite

It’s Time to Join Stryker!

 

Why Join Us

In this role, you will help strengthen software quality practices across a growing portfolio of digital and connected solutions. You will work with software teams to improve lifecycle quality, support audit readiness, and enable compliant, efficient software delivery.


Stryker is seeking a Staff Software Quality Assurance Engineer to support our Digital Platform Hub. In this role, you will partner with software R&D teams to implement and improve quality processes across digital, connected, SaaS, and cloud-based products.


You will provide quality guidance throughout the software development lifecycle, support audit and compliance readiness, and help translate regulatory and industry requirements into practical, scalable processes.


This is not a software testing or test-execution role. This position focuses on software quality systems, SDLC governance, risk management, audit readiness, and process improvement.


What You Will Do

 

Software Quality Systems and Lifecycle Support
  • Guide software teams through applicable Quality Management System processes, procedures, and documentation requirements.
  • Develop and improve software quality procedures, work instructions, templates, and guidance documents.
  • Provide quality support across requirements, design, development, testing, release, operations, and software change-management activities.
  • Participate in design reviews, risk assessments, change assessments, and release-readiness activities.
  • Help ensure software quality and compliance risks are identified, documented, and appropriately addressed.
  • Support quality practices within Agile, DevOps, and CI/CD environments.

Audit and Compliance Readiness
  • Support SOC 2, ISO 27001, HIPAA, FDA, and other applicable compliance and audit-readiness activities.
  • Partner with control owners to ensure controls are maintained and supported by appropriate evidence.
  • Support internal and external audits through gap assessments, evidence collection, remediation, and audit preparation.
  • Participate in investigations, root-cause analysis, corrective actions, and effectiveness monitoring.

Cross-Functional Partnership and Process Improvement
  • Partner with Software Engineering, Test Engineering, Product Security, Privacy, Regulatory Affairs, IT, Operations, and Quality.
  • Identify process gaps and support improvements that strengthen consistency, efficiency, and compliance.
  • Translate quality, regulatory, security, and compliance requirements into practical development processes.
  • Influence cross-functional stakeholders and help resolve conflicts between development priorities and quality requirements.

 

What You Need
  • Bachelor’s degree in Software Engineering, Computer Science, Engineering, Quality, or a related technical discipline is required
  • Four or more years of professional experience in software quality, quality systems, software compliance, audit, or a related field supporting software, SaaS, cloud-based, or connected products is required
  • Experience developing, implementing, maintaining, or improving software quality processes or procedures is required.

Preferred Qualifications
  • Master’s degree or another advanced technical degree.
  • Professional experience in software engineering or development before transitioning into software quality, compliance, or quality systems.
  • Strong understanding of the software development lifecycle, including change control, risk management, audit readiness, and Quality Management System processes.
  • Experience partnering with software development or R&D teams to implement or improve software quality processes.
  • Experience supporting regulated software products, preferably within medical devices, digital health, healthcare technology, or another compliance-driven industry.
  • Experience with SOC 2, ISO 27001, HIPAA, FDA software expectations, 21 CFR Part 11, IEC 62304, ISO 14971, ISO 13485, or comparable frameworks.
  • Working knowledge of cloud platforms, DevOps, CI/CD, and software security controls.
  • Experience supporting audits, gap assessments, remediation activities, quality investigations, or corrective and preventive actions.
  • Demonstrated ability to influence cross-functional teams, communicate complex requirements, and support process improvements without direct authority.
  • Professional certification such as CSQE, CQE, CQA, or an equivalent quality or compliance credential.

  


United States of America Pay Ranges:

  • USN: $102,600 - $171,000 USD Annual
  • US5: $107,700 - $179,600 USD Annual
  • US10: $112,900 - $188,100 USD Annual
  • US15: $118,000 - $196,600 USD Annual
  • US20: $123,100 - $205,200 USD Annual
  • US30: $133,400 - $222,300 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

  


Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills Required

  • Bachelor's degree in Software Engineering, Computer Science, Engineering, Quality, or a related technical discipline
  • Four or more years of professional experience in software quality, quality systems, software compliance, audit, or a related field supporting software, SaaS, cloud-based, or connected products
  • Experience developing, implementing, maintaining, or improving software quality processes or procedures
  • Master's degree or another advanced technical degree
  • Professional experience in software engineering or development before transitioning into software quality, compliance, or quality systems
  • Strong understanding of the software development lifecycle, change control, risk management, audit readiness, and Quality Management System processes
  • Experience partnering with software development or R&D teams to implement or improve software quality processes
  • Experience supporting regulated software products, preferably within medical devices, digital health, healthcare technology, or another compliance-driven industry
  • Experience with SOC 2, ISO 27001, HIPAA, FDA software expectations, 21 CFR Part 11, IEC 62304, ISO 14971, ISO 13485, or comparable frameworks
  • Working knowledge of cloud platforms, DevOps, CI/CD, and software security controls
  • Experience supporting audits, gap assessments, remediation activities, quality investigations, or corrective and preventive actions
  • Ability to influence cross-functional teams, communicate complex requirements, and support process improvements without direct authority
  • Professional certification such as CSQE, CQE, CQA, or an equivalent quality or compliance credential

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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