Full-Time

Prin Software Design Quality Embedded

Confirmed live in the last 24 hours

Medtronic

Medtronic

10,001+ employees

Develops and manufactures medical devices and therapies

Biotechnology
Healthcare

Compensation Overview

$119.2k - $178.8kAnnually

+ Short-term Incentive (Medtronic Incentive Plan)

Senior, Expert

Los Angeles, CA, USA + 1 more

More locations: San Diego, CA, USA

Category
Embedded Engineering
Software Engineering
Required Skills
Git
JUnit
JIRA
Jenkins
SCRUM
Selenium
Requirements
  • Bachelors Degree in Engineering, Science or Technical Field with 7+ years of experience in Engineering, Software Development and/or Quality
  • OR Advanced Degree Engineering, Science or Technical Field with 5+ years of experience in Engineering, Software Development and/or Quality
  • Experience in software design and development, verification, validation and testing activities.
  • Experience executing in the SDLC environment leveraging ALM tools (Eg: PTC Integrity/Atlassian Suite/TFS), defect tracking tools (Eg:Jira), development tools (Git, SourceTree, Android Studio, GitLab), test tools (Selenium/JUnit), CI/CD tools (Jenkins).
  • Exposure to medical device compliance standards (such as ISO13485/IEC62304/HIPAA/FDA/Security Standards/Data Privacy).
  • Ability to author technical reports, business correspondence and standard operating procedures.
  • Exposure in data driven insight solutions leveraging machine learning/artificial intelligence (AI).
  • Exposure with wireless communication protocols (Eg: Bluetooth).
  • Exposure to n-tier architecture models and/or experience with ITIL processes/IT systems.
  • Working knowledge of integrated digital health systems including consumer products such as Apple Inc./Android products.
  • Certified scrum master or SAFe or Black Belt or Green Belt or CQE preferred.
Responsibilities
  • Lead as a quality core/extended team member responsible for driving quality into the embedded software solutions in accordance with IEC 62304.
  • Lead the collaborative quality strategy for projects in alignment with business goals for cross-functional teams including R&D/Regulatory/Marketing/Operations.
  • Lead quality focused design and development of software within the software development lifecycle (Agile/waterfall/ SAFe/DevOps) by defining the requirements, design, verification and validation plan and strategies while maintaining traceability.
  • Participate in design reviews for the system as well as review and approve design input/design output artifacts including requirements, design documents, code review reports, test results, verification and validation reports and defects.
  • Conduct risk management activities including system risk analysis (ISO14971) and software FMEA’s.
  • Drive CAPA (Corrective and Preventative Action) projects.
  • Participate in both internal and external regulatory audits and inspections.
  • Lead quality improvement projects to include compliance standards for software quality operating methods, processes, and procedures (such as ISO13485/IEC62304/HIPAA/FDA/Security Standards/Data Privacy).
  • Define appropriate metrics to measure product quality and drive reliability.
  • Develops, modifies, applies, and maintains standards for software systems quality operating methods, processes, and procedures.
  • Conducts evaluation of software systems activities including requirements, design, development, documentation, integration, test, verification and validation.
  • Defines appropriate measures to ensure product quality.
  • Develops overall operating criteria to ensure implementation of the software quality program according to project, process and contract requirements and objectives.
  • Ensures that projects and process control documentation are compliant with requirements, objectives and/or contracts.
  • Reviews software systems design, change specifications, and plans against contractual and/or process requirements.
  • Reviews include applicable specifications, materials, tools, techniques, and methodologies.
  • Provides or directs verification and validation of software system requirements, traceability, and testability.

Medtronic provides medical technology, services, and solutions to improve patient care. The company develops a variety of medical devices, including pacemakers, insulin pumps, surgical tools, and neurostimulation devices, which help diagnose, prevent, and treat chronic diseases. These products are used by hospitals and healthcare professionals around the world. Medtronic stands out from competitors by not only focusing on product development but also offering comprehensive services such as training for healthcare providers and patient management programs. The goal of Medtronic is to enhance patient outcomes and lower healthcare costs through its advanced medical solutions.

Company Stage

IPO

Total Funding

$3.2M

Headquarters

Fridley, Minnesota

Founded

1949

Simplify Jobs

Simplify's Take

What believers are saying

  • Increased adoption of telehealth drives demand for Medtronic's connected medical devices.
  • Rise in personalized medicine creates opportunities for customized Medtronic devices.
  • Focus on value-based healthcare aligns with Medtronic's cost-reducing technologies.

What critics are saying

  • Emerging medtech companies like Anteris could challenge Medtronic's market share.
  • Growing spine biologics market may disrupt Medtronic's existing product lines.
  • Departure of key personnel like Ira Bindra could impact organizational stability.

What makes Medtronic unique

  • Medtronic is a global leader in medical technology, operating in over 150 countries.
  • The company offers a comprehensive suite of products and services for chronic diseases.
  • Medtronic invests heavily in R&D to innovate and bring new products to market.

Help us improve and share your feedback! Did you find this helpful?