Job Title: Software Quality Assurance Engineer

Job Description

We are seeking a dedicated and detail-oriented Software Quality Assurance Engineer to join our team. This role involves designing, developing, and implementing quality assurance procedures for our software products, ensuring they comply with regulatory standards and meet high-quality performance metrics. The ideal candidate will work closely with product teams to monitor and improve software performance, review documentation for regulatory submissions, and stay updated with industry trends and best practices.

ResponsibilitiesDesign, 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, 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.Essential SkillsExperience in software quality assurance and validation.Background in medical devices or diagnostics, especially DNA sequencing.Knowledge of FDA compliance and documentation, including FDA 21 CFR Part 820.Proficiency in verification and validation (V&V) processes.Strong knowledge of IEC, ISO-IEC, and ISO standards.Bachelor’s Degree or equivalent in Computer Science, Engineering, or a related field.Moderate experience in a software regulatory environment or medical device software development.Additional Skills & QualificationsExcellent decision-making and problem-solving skills using quality tools.Exceptional verbal, written, and organizational skills.Ability to work effectively in a fast-paced, start-up environment.Work Environment

Our team offers a collaborative and innovative work environment with benefits that include 3 weeks of PTO, sick pay accrual up to 80 hours, and a 2% match on our 401(k) with no vesting period. The position requires working closely with product and regulatory teams, ensuring compliance and high-quality standards in all software products.

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 for other accommodation options.