{"schemaVersion":"jobsearcher.job.v1","id":"7a232e717853593403aecc80","url":"https://jobsearcher.com/jobs/7a232e717853593403aecc80","canonicalUrl":"https://jobsearcher.com/jobs/7a232e717853593403aecc80","title":"Systems Engineer - Software","description":"Employment Type: W2 / 1 Year Contract with possibility of extensions!\nPay Rate: $39.00 – $42.00 per hour (Based on experience, paid weekly)\nBenefits: Medical, Dental, Vision, and Life Insurance\nNote: This is an onsite position.\n\nBEPC Inc. - Business Excellence Professional Consulting provided pay range\nThis range is provided by BEPC Inc. - Business Excellence Professional Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.\n\nBase pay range\n$39.00/hr - $42.00/hr\n\nRole Overview\nBEPC, Inc. is actively seeking a Systems Engineer – Software to support our client, a global leader in cancer diagnostics, located in Tucson, AZ. This role focuses on software product definition, requirements development, system design, and risk analysis for regulated medical device systems used in diagnostic applications.\n\nThe ideal candidate will have experience in software requirements engineering, risk management, and system-level analysis, with a strong understanding of IVD and FDA-regulated environments. This position offers an exciting opportunity to advance innovations in automated cancer testing and life‑saving diagnostic technologies.\n\nKey Responsibilities\n\nSystem Lifecycle Management: Apply Systems Engineering principles to software product definition, requirements documentation, risk analysis, and system validation.\n\nSoftware Product Development: Author, review, and manage software requirements , ensuring traceability and compliance with quality and regulatory standards.\n\nRisk & Compliance Management: Conduct software risk analyses in alignment with FDA , ISO 13485 , and IEC 62304 standards.\n\nCross-Functional Collaboration: Work collaboratively across R&D, Quality, Regulatory, Operations, and Marketing to translate business and technical needs into actionable system requirements.\n\nSystem Architecture Design: Support the design of robust, scalable, and compliant software architectures.\n\nTrade‑Off Analysis: Perform design and performance trade‑offs to optimize software functionality, reliability, and usability.\n\nTesting & Validation: Participate in verification and validation (V&V) activities to confirm compliance with system and regulatory requirements.\n\nContinuous Improvement: Identify and implement process improvements to streamline development, testing, and documentation workflows.\n\nTechnical Leadership: Serve as a subject matter expert in systems and software integration, providing mentorship and guidance on risk management and compliance.\n\nQualifications\nEducation:\n\nBachelor’s degree in Engineering, Biomedical Sciences, Computer Science, or a related technical field with at least 4 years of experience or Master’s degree with 2 years of experience or PhD in a relevant discipline.\n\nExperience:\n\nProven background in software systems engineering , requirements writing , and risk analysis .\n\n2–4 years of experience in a regulated medical device or IVD environment required.\n\nStrong understanding of system lifecycle management , software verification/validation , and configuration management .\n\nTechnical Skills:\n\nExperience with requirements management tools (e.g., DOORS, Jama, or similar).\n\nFamiliarity with risk management frameworks (ISO 14971).\n\nWorking knowledge of FDA 21 CFR Part 820 , ISO 13485 , and IEC 62304 .\n\nProficiency in software integration and testing .\n\nSoft Skills:\n\nExcellent written and verbal communication skills.\n\nStrong organizational and time management abilities to manage multiple projects.\n\nCollaborative mindset and the ability to influence cross‑functional teams.\n\nPreferred Qualifications:\n\nAdvanced understanding of software reliability, manufacturability, and usability .\n\nExperience in software architecture and system modeling .\n\nFamiliarity with emerging IVD and diagnostic technologies .\n\nStrong analytical skills and ability to drive root cause analysis and risk mitigation .\n\nSeniority level\nNot Applicable\n\nEmployment type\nContract\n\nJob function\nBiotechnology Research and Pharmaceutical Manufacturing\n\nReferrals increase your chances of interviewing at BEPC Inc. - Business Excellence Professional Consulting by 2x\n\n#J-18808-Ljbffr","company":"Bepc","rawCompany":"bepc","city":"Tucson","state":"AZ","isRemote":false,"isActive":false,"createdAt":"2026-07-16T04:03:33.480Z","occupations":[{"code":"15-1252.00","title":"Software Developers","slug":"software-developers"},{"code":"15-1299.08","title":"Computer Systems Engineers/Architects","slug":"computer-systems-engineers-architects"},{"code":"15-1211.00","title":"Computer Systems Analysts","slug":"computer-systems-analysts"}],"industries":[{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"},{"code":"541511","title":"Custom Computer Programming Services","slug":"custom-computer-programming-services"},{"code":"513210","title":"Software Publishers","slug":"software-publishers"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Systems Engineer - Software","description":"Employment Type: W2 / 1 Year Contract with possibility of extensions!\nPay Rate: $39.00 – $42.00 per hour (Based on experience, paid weekly)\nBenefits: Medical, Dental, Vision, and Life Insurance\nNote: This is an onsite position.\n\nBEPC Inc. - Business Excellence Professional Consulting provided pay range\nThis range is provided by BEPC Inc. - Business Excellence Professional Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.\n\nBase pay range\n$39.00/hr - $42.00/hr\n\nRole Overview\nBEPC, Inc. is actively seeking a Systems Engineer – Software to support our client, a global leader in cancer diagnostics, located in Tucson, AZ. This role focuses on software product definition, requirements development, system design, and risk analysis for regulated medical device systems used in diagnostic applications.\n\nThe ideal candidate will have experience in software requirements engineering, risk management, and system-level analysis, with a strong understanding of IVD and FDA-regulated environments. This position offers an exciting opportunity to advance innovations in automated cancer testing and life‑saving diagnostic technologies.\n\nKey Responsibilities\n\nSystem Lifecycle Management: Apply Systems Engineering principles to software product definition, requirements documentation, risk analysis, and system validation.\n\nSoftware Product Development: Author, review, and manage software requirements , ensuring traceability and compliance with quality and regulatory standards.\n\nRisk & Compliance Management: Conduct software risk analyses in alignment with FDA , ISO 13485 , and IEC 62304 standards.\n\nCross-Functional Collaboration: Work collaboratively across R&D, Quality, Regulatory, Operations, and Marketing to translate business and technical needs into actionable system requirements.\n\nSystem Architecture Design: Support the design of robust, scalable, and compliant software architectures.\n\nTrade‑Off Analysis: Perform design and performance trade‑offs to optimize software functionality, reliability, and usability.\n\nTesting & Validation: Participate in verification and validation (V&V) activities to confirm compliance with system and regulatory requirements.\n\nContinuous Improvement: Identify and implement process improvements to streamline development, testing, and documentation workflows.\n\nTechnical Leadership: Serve as a subject matter expert in systems and software integration, providing mentorship and guidance on risk management and compliance.\n\nQualifications\nEducation:\n\nBachelor’s degree in Engineering, Biomedical Sciences, Computer Science, or a related technical field with at least 4 years of experience or Master’s degree with 2 years of experience or PhD in a relevant discipline.\n\nExperience:\n\nProven background in software systems engineering , requirements writing , and risk analysis .\n\n2–4 years of experience in a regulated medical device or IVD environment required.\n\nStrong understanding of system lifecycle management , software verification/validation , and configuration management .\n\nTechnical Skills:\n\nExperience with requirements management tools (e.g., DOORS, Jama, or similar).\n\nFamiliarity with risk management frameworks (ISO 14971).\n\nWorking knowledge of FDA 21 CFR Part 820 , ISO 13485 , and IEC 62304 .\n\nProficiency in software integration and testing .\n\nSoft Skills:\n\nExcellent written and verbal communication skills.\n\nStrong organizational and time management abilities to manage multiple projects.\n\nCollaborative mindset and the ability to influence cross‑functional teams.\n\nPreferred Qualifications:\n\nAdvanced understanding of software reliability, manufacturability, and usability .\n\nExperience in software architecture and system modeling .\n\nFamiliarity with emerging IVD and diagnostic technologies .\n\nStrong analytical skills and ability to drive root cause analysis and risk mitigation .\n\nSeniority level\nNot Applicable\n\nEmployment type\nContract\n\nJob function\nBiotechnology Research and Pharmaceutical Manufacturing\n\nReferrals increase your chances of interviewing at BEPC Inc. - Business Excellence Professional Consulting by 2x\n\n#J-18808-Ljbffr","datePosted":"2026-07-16T04:03:33.480Z","dateModified":"2026-07-16T04:03:33.480Z","hiringOrganization":{"@type":"Organization","name":"Bepc","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Tucson","addressRegion":"AZ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"7a232e717853593403aecc80"},"url":"https://jobsearcher.com/jobs/7a232e717853593403aecc80"}}