Medical Device Software Engineer

4 weeks ago

Indianola, United States Rose International Full time

This Medical Device Software Engineer will be responsible to perform software development of medical devices to deliver a high-quality product that meets or exceeds customer expectations and meets FDA design controls.

Education Requirements:

Bachelor’s degree in computer engineering, Electronics, or Electrical Engineering

Requirements for the Software Engineer:

Minimum of 5 years of relevant work experience in software engineering including all phases of SDLC

Good understanding of software development processes, software architecture and data structure.

Minimum of 5 years of experience in programming languages and framework: C++, QT/QML and Python.

Minimum of 2 years of experience in gRPC framework.

Working knowledge of tools and technologies including GitHub, Jira, Confluence, Artifactory, SonarQube, CI/CD GitHub pipelines.

Working knowledge on OS such as Windows, Linux flavors preferably Ubuntu.

Must be able to manage multiple tasks and manage priorities accordingly.

Position Description:

- You will be involved in all aspects of the product development lifecycle from requirements to delivery in an agile scrum framework.

- You will work closely with the Bayer product managers, and various cross functional teams to deliver world-class solutions to Bayer customers.

- You will design and develop high-quality medical devices exhibiting excellent performance that meets product requirements and exceeds customer satisfaction.

Medical Device Software Engineer Responsibilities:

Think big; bring fresh ideas and approaches to design and develop innovative solutions in medical device to meet or exceed customer satisfaction

Evaluate different design choices, prototype new technology, and implement technical solutions

Understand business impact of design choices, and make technical trade-offs using sound judgement

Adopt engineering best practices around software development

Achieve understanding of product requirement and software requirement to design and develop medical device and improve customer value

Achieve understanding of software risk analysis and its impact on design and implementation of medical device

Deliver high-quality and scalable architecture designs and code

Design and develop applications and services using SDLC process for medical device development.

Identify opportunities to develop new and better solutions.

Participate in code reviews of other software engineers, and design reviews

Develop any technical documentation needed to accurately represent application design and code.

Ensures the development initiatives of Bayer Radiology medical devices complies and adheres to Bayer Standard Operating Procedures that meets regulatory standards and guidance such as

o FDA 21 CFR 820.30 – Design Controls

o FDA Cybersecurity in Medical Devices

o IEC 62304 – Software in a Medical Device

Effectively collaborates within cross-functional teams across multiple geographies to convey problems, opportunities, solutions, and results in the medical device development

Manages own work activities to given objectives
  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**

Benefits:

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

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