Software Quality Engineer 2
Pharma
Job description
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Position Summary: Software Quality Engineer 2 provides support to Illumina’s software development teams to ensure product software is developed in compliance with Illumina’s policies/procedures and applicable regulatory requirements ( e.g., 21CFR820, QMSR ) and International Standards ( e.g., ISO 13485 , IEC 62304 ) . The role supports execution of software quality activities across assigned program (s) , ensuring deliverables are completed on time and in compliance with established processes. The engineer works closely with cross-functional teams and contributes to continuous improvement of software quality practices. Tasks and Responsibilities: Provide software quality support across the Software Development Life Cycle (SDLC) for assigned program (s) Collaborate with cross-functional teams (Software Development, Program Management, Product Security, etc.) to support execution of quality activities Provide support on software development projects through review and approval of deliverables , including : Software Development Plans, Verification Plans, Validation Plans Product/Software Requirements Software Architectural and Design Documents Test Protocols, Requirement Traceability Matrix, Test Reports Cybersecurity and risk-related documentation Assist teams in determining verification and validation needs and requirements Participate in software risk management activities throughout the product lifecycle Participate in design reviews to support effective development, transfer, and maintenance of software products Provide support for software-related quality issues (e.g., complaints, CAPA), including investigation and resolution activities Identify opportunities for process improvements and support implementation of continuous improvements in the Software Quality Program Support development and delivery of training on software quality processes and practices Provide support for new technology areas (e.g., AI/ML, Cybersecurity, Cloud) as applicable to software systems and tools Support internal and external audits related to product software and software quality processes Escalate risks and issues as appropriate to ensure timely visibility and resolution Support other areas of the Quality System and perform additional tasks as defined by management All listed tasks and responsibilities are deemed essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities. Preferred Education: Bachelor’s degree in C omputer S cience , Software Engineering, Bioinformatics , Biomedical or related discipline Job Requirements : 2+ years’ experience in (software) quality engineering or related role in a regulated industry Working knowledge of applicable industry standards and regulations ( e . g ., IEC 62304, ISO 13485 , 21 CFR ) Basic understanding of software development lifecycle (SDLC) processes and software engineering best practices Ability to execute assigned quality tasks with guidance a
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