Actalent
Software Quality Assurance Engineer
Actalent, Carlsbad, California, United States, 92002
Job Title: Software Quality Assurance Engineer
Job Description
Responsibilities:
• Design, develop, and implement quality assurance standard operating procedures and processes for all software products to comply with regulatory bodies.
• Review and approve test plans and test cases to ensure that software meets desired quality and performance standards.
• Issue test record documents to perform software verification by software test engineers.
• Develop requirement traceability metrics (from user requirements to functional requirements).
• Review and approve software documentation for regulatory submission requirements.
• Facilitate design input, design lock, and software release ceremonies.
• Review and approve software-related risk documentation (Safety, Security, and Usability).
• Establish metrics to measure the quality and performance of existing and new software products.
• Monitor and analyze software performance, user feedback, and defects to identify areas for improvement.
• Work with product teams to ensure that software meets business and user requirements.
• Review verification reports at the end of each release.
• Review Software Bill of Materials (SBOM) to ensure all Software of Unknown Provenance (SOUP) tools or packages are up to date.
• Own software-related FDA 510(k) submission documents.
• Participate in the design and review of software architecture.
• Keep up to date with industry trends and best practices.
Hard Skills
Medical Device or Diagnostics (DNA sequencing)
SW Quality
V&V
FDA Docs
Job Type
This is a permanent position.
Work Site
This is a fully on-site position in CARLSBAD, California.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
Responsibilities:
• Design, develop, and implement quality assurance standard operating procedures and processes for all software products to comply with regulatory bodies.
• Review and approve test plans and test cases to ensure that software meets desired quality and performance standards.
• Issue test record documents to perform software verification by software test engineers.
• Develop requirement traceability metrics (from user requirements to functional requirements).
• Review and approve software documentation for regulatory submission requirements.
• Facilitate design input, design lock, and software release ceremonies.
• Review and approve software-related risk documentation (Safety, Security, and Usability).
• Establish metrics to measure the quality and performance of existing and new software products.
• Monitor and analyze software performance, user feedback, and defects to identify areas for improvement.
• Work with product teams to ensure that software meets business and user requirements.
• Review verification reports at the end of each release.
• Review Software Bill of Materials (SBOM) to ensure all Software of Unknown Provenance (SOUP) tools or packages are up to date.
• Own software-related FDA 510(k) submission documents.
• Participate in the design and review of software architecture.
• Keep up to date with industry trends and best practices.
Hard Skills
Medical Device or Diagnostics (DNA sequencing)
SW Quality
V&V
FDA Docs
Job Type
This is a permanent position.
Work Site
This is a fully on-site position in CARLSBAD, California.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.