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Job Description:
Sr. Software Quality Engineer
needed for a contract opportunity with Yoh Scientific’s client located in
San Diego, CA. This position is for a
biotech company , and the team is looking for candidates with a
minimum of 5 years of experience in Software Quality Engineering, preferably within multi-omics or bioinformatics. Schedule:
Hybrid, 40 hours a week, Monday – Friday. Responsibilities: Own all aspects of Software Design Quality for IVDR and RUO software, including risk management, design controls, and Design History File (DHF). Provide Software Quality Engineering support for project planning, requirements/specification development, software verification, design verification and validation, design transfer, process development, process validation, risk management, and/or human factors. Own risk management activities, including the Risk Management File (RMF), risk management plan, hazard analysis, dFMEA, and risk management report. Serve as the SME for Software Quality Engineering and collaborate with teams on code reviews, software security analysis, defect and vulnerability triage, creation and maintenance of sBOMs, etc., and lead the implementation of best practices for software quality processes. Drive cross functional engagement with cross-functional stakeholders to optimize the success of development projects. Support audits to ensure the quality and completeness of product DHFs Conduct root cause investigations of product complaints and quality issues, initiate corrective actions, and monitor the implementation and effectiveness of corrective actions, when applicable. Support other areas of company’s Quality Management System (QMS), when applicable. Qualifications: Bachelor's Degree or Master's Degree in Engineering, Bioengineering, Bioinformatics, Computer Science, or related engineering field. 5+ years of experience in Software Quality Engineering experience, preferably within multiomics or bioinformatics. Strong understanding of international medical device/IVDR regulations and standards, including 21 CFR 820, ISO 13485, IEC 62304, and ISO 14971. Strong understanding of software developmental best practices for digital health software, Medical Device Data Systems, and cloud-based software/systems. Organized self-starter, able to work in a fast-paced environment. Exceptional analytical and problem-solving skills. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, national origin, age, disability, or status as a protected veteran. Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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Sr. Software Quality Engineer
needed for a contract opportunity with Yoh Scientific’s client located in
San Diego, CA. This position is for a
biotech company , and the team is looking for candidates with a
minimum of 5 years of experience in Software Quality Engineering, preferably within multi-omics or bioinformatics. Schedule:
Hybrid, 40 hours a week, Monday – Friday. Responsibilities: Own all aspects of Software Design Quality for IVDR and RUO software, including risk management, design controls, and Design History File (DHF). Provide Software Quality Engineering support for project planning, requirements/specification development, software verification, design verification and validation, design transfer, process development, process validation, risk management, and/or human factors. Own risk management activities, including the Risk Management File (RMF), risk management plan, hazard analysis, dFMEA, and risk management report. Serve as the SME for Software Quality Engineering and collaborate with teams on code reviews, software security analysis, defect and vulnerability triage, creation and maintenance of sBOMs, etc., and lead the implementation of best practices for software quality processes. Drive cross functional engagement with cross-functional stakeholders to optimize the success of development projects. Support audits to ensure the quality and completeness of product DHFs Conduct root cause investigations of product complaints and quality issues, initiate corrective actions, and monitor the implementation and effectiveness of corrective actions, when applicable. Support other areas of company’s Quality Management System (QMS), when applicable. Qualifications: Bachelor's Degree or Master's Degree in Engineering, Bioengineering, Bioinformatics, Computer Science, or related engineering field. 5+ years of experience in Software Quality Engineering experience, preferably within multiomics or bioinformatics. Strong understanding of international medical device/IVDR regulations and standards, including 21 CFR 820, ISO 13485, IEC 62304, and ISO 14971. Strong understanding of software developmental best practices for digital health software, Medical Device Data Systems, and cloud-based software/systems. Organized self-starter, able to work in a fast-paced environment. Exceptional analytical and problem-solving skills. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, national origin, age, disability, or status as a protected veteran. Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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