Becton, Dickinson and Company

Sr. Software Quality Engineer

Becton, Dickinson and Company$105K — $168K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or related technical field; Master's preferred.
  • 5+ years in software quality assurance; at least 2 years in medical devices or regulated environment.
  • Strong grasp of SDLC methodologies like Agile and Waterfall in a regulated context.
  • In-depth knowledge of medical device regulations, including FDA QSR, ISO 13485, and IEC 62304.
  • Experience designing, implementing, and executing diverse software tests.
  • Proficiency with test management tools (Polarion, Jira, Azure DevOps); Polarion experience is a plus.
  • Experience with automated testing tools like Selenium is highly desirable.

Responsibilities

  • Develop and maintain software quality assurance strategies and procedures per industry standards.
  • Lead SWQA efforts for new product development projects.
  • Understand software risks and create associated risk management documentation.
  • Facilitate defect management and CCB meetings to address project defects.
  • Conduct design reviews and code assessments to catch quality issues early.
  • Define test plans and conduct various testing levels (unit, integration, system, regression).
  • Collaborate with cross-functional teams to integrate quality activities throughout the product lifecycle.

Benefits

  • Comprehensive Total Rewards program supporting employee development.
  • Performance-based recognition opportunities.
  • Competitive compensation package.
  • Commitment to attracting and retaining high-quality talent.
Full Job Description

Job Summary
As a Sr. Software Quality Engineer at Becton, Dickinson and Company, you will play a critical role in ensuring the quality and reliability of our medical device software. You will be responsible for defining, implementing, and executing robust quality assurance processes throughout the entire software development lifecycle, contributing to the delivery of safe and effective products that positively impact patient care.

Job Responsibilities

  • Develop, implement, and maintain comprehensive software quality assurance strategies, plans, and procedures in accordance with industry best practices and regulatory requirements (e.g., FDA, ISO 13485, IEC 62304).

  • Experience in being lead SWQA for new product development projects.

  • Ability to understand software risks and develop risk management files for software and system level risk.

  • Lead defect management and CCB meetings to review and disposition project defects

  • Lead and participate in design reviews, code reviews, and other technical assessments to identify potential quality issues early in the development process.

  • Understanding of test plans, test cases, and test scripts for various levels of testing, including unit, integration, system, and regression testing.

  • Perform risk analysis and develop mitigation strategies for software defects and quality-related issues.

  • Understanding of complaints process and metrics

  • Collaborate closely with software development, project management, and regulatory affairs teams to ensure seamless integration of quality activities throughout the product lifecycle.

  • Investigate, analyze, and document software defects, working with development teams to ensure timely resolution and verification.

  • Contribute to the continuous improvement of software development processes and quality assurance methodologies.

  • Participate in external and internal audits, providing documentation and expertise related to software quality.

  • Stay current with emerging technologies, industry trends, and regulatory changes in medical device software quality.


Job Qualifications

  • Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related technical field. Master's degree preferred.

  • 5+ years of experience in software quality assurance, with at least 2 years in the medical device industry or another highly regulated environment.

  • Strong understanding of software development lifecycle (SDLC) methodologies (e.g., Agile, Waterfall) and their application in a regulated context.

  • In-depth knowledge of relevant medical device regulations and standards, including FDA 21 CFR Part 820 (QSR), ISO 13485, and IEC 62304.

  • Proven experience in designing, implementing, and executing various types of software testing.

  • Proficiency with test management tools (e.g., Polarion, Jira, Azure DevOps) and defect tracking systems. Polarion knowledge is a plus.

  • Experience with automated testing frameworks and tools (e.g., Selenium, Coded UI, Squish) is highly desirable.

  • Excellent analytical, problem-solving, and critical thinking skills.

  • Strong communication (written and verbal) and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.

  • Ability to work independently and as part of a team in a fast-paced, dynamic environment.

Required Skills

Optional Skills

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Primary Work LocationUSA CA - Irvine Laguna Canyon

Additional Locations

Work Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$105,500.00 - $168,800.00 USD Annual

About Becton, Dickinson and Company

BD is a global technology company that provides diagnostics and technologies for frontliners. Through their solutions and services, they assist scientists in detecting diseases and advanced researchers' on developing diagnoses and therapeutics. BD was established in 1897 by Farleigh Dickinson and Maxwell Becton in East Rutherford, New Jersey.

Becton, Dickinson and Company Careers

Join the innovative world of Becton, Dickinson and Company (BD), a global medical technology company that is actively seeking driven, dedicated professionals to join our team. At BD, we are committed to advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. This commitment provides the foundation for a workplace where you can engage in meaningful work and where job opportunities abound.

Work You’ll Do

At BD, you will be part of a culture that values diversity, leadership, and innovation. Our team members are empowered to lead and inspire from day one. Join us and contribute to our mission of advancing the world of health through your professional skills and personal passion.

Transform Your Career

BD offers a unique position in the marketplace that combines industry expertise, leadership in medical innovation, and a collaborative culture to help you grow your career. Whether you are looking for an entry-level position or a more senior role, we provide the tools and support for your professional growth through comprehensive training and development programs.

Innovative Work Environment

Our team at BD is composed of more than 65,000 associates across the globe. These dedicated professionals work at the intersection of technology and healthcare, where they drive innovation and ensure that we stay ahead in a rapidly evolving industry. By joining BD, you will work alongside some of the brightest minds in the industry.

Internship and Employment Opportunities

Start your career with BD through our internship programs or dive straight into a full-time position. We offer a range of opportunities that allow you to explore different areas of our business and find a path that aligns with your career goals. Our hiring process is designed to be transparent and engaging, ensuring that all candidates—whether submitting a resume for an internship or a senior position—feel valued and informed.

Benefits and Culture

BD is proud to offer competitive benefits that support the health, well-being, and financial security of our employees and their families. From comprehensive health insurance to employee wellness programs and flexible working arrangements, we prioritize the well-being of our team members. Our inclusive culture encourages networking, continuous learning, and the sharing of ideas in a diverse and welcoming environment.

Join Our Team

Explore the job opportunities at BD and discover how your expertise can help shape the future of healthcare. Search open positions that match your skills and interests. We look for passionate, curious, creative, and solution-driven team players.

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Explore Careers at BD

Whether you're preparing for your first interview or looking to advance into a leadership role, BD offers career paths that foster continuous growth and innovation. Join us in our mission to improve medical outcomes and enhance patient care worldwide.

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At Becton, Dickinson and Company, we are more than just a company; we are a community that is dedicated to making a difference in the lives of people all around the world.
Learn more about Becton, Dickinson and Company
Size
75,000 employees
Market Cap
$72 billion
Industry
Net Income
$1.6 billion
Founded
1897
5 Year Trend
+9.3%
Revenue
$18.2 billion
NASDAQ

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