Job Title: Software Quality Assurance Engineer
Job Description

We are seeking a highly skilled and motivated Software Quality Assurance Engineer to design, develop, and implement quality assurance standard operating procedures and processes for all software products. This role will ensure compliance with regulatory bodies and maintain high-quality standards throughout the software development lifecycle.

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, 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.Essential SkillsMedical device experienceFDA ComplianceRisk managementSoftware quality managementDesign controlCompliance on product software - lead development, testing, and verification documentation (risk management, V&V, writing documentation for submission)Understanding of the software development lifecycle and ensuring compliance across the entire lifecycleFDA documentationExperience with diagnostic instruments, procedure writing, and auditsAdditional Skills & QualificationsBachelor’s Degree or equivalent in Computer Science, Engineering, or related fieldModerate experience in software regulatory environment/medical device software developmentStrong knowledge of IEC, ISO-IEC, ISO, FDA 21 CFR Part 820Excellent decision-making skills, proficient in providing solutions for complex challenges, and good problem-solving using quality toolsExceptional verbal, written, and organizational skillsAbility to work effectively in a fast-paced, start-up environmentWork Environment

This role offers a dynamic and collaborative work environment within a fast-paced, start-up setting. Employees will benefit from 3 weeks of PTO, sick pay accrual up to 80 hours, and a 2% match on our 401(k) with no vesting period. The work environment emphasizes continuous learning and staying updated with industry trends and best practices.

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.