Jobs via Dice
Systems Engineer - Assay Development with cytology specimens
Jobs via Dice, Tucson, Arizona, United States, 85718
Job Title
Systems Engineer - Assay Development with cytology specimens (Hybrid) Location: Tucson, AZ Duration: 12+ months Pay: $40.00/hr - $45.00/hr (base pay range) Responsibilities
Drive requirements definition, risk management, and verification & validation practices in projects. Define requirements, design system architectures, and implement solutions to meet IVD standards. Take ownership of project deliverables and facilitate decision-making with well-considered tradeoffs. Work cross-functionally with many stakeholders, balancing needs and tradeoffs to reach aligned outcomes. Qualifications
MUST HAVE
Requirement writing experience in a regulated industry (medical device industry preferred). Risk analysis (FMEA) experience in an engineering discipline (regulated medical device company preferred). Demonstrated knowledge of systems engineering principles, including requirements engineering, tradeoff analysis, risk management, configuration management, and verification & validation. Ability to work cross-functionally with many stakeholders and achieve alignment on needs and tradeoffs. IDEAL
Assay development experience, particularly with cytology specimens. Prior experience in RETINA (Requirements & Test Integration Application) and with LucidSpark/LucidChart. Excellent organizational skills with the ability to evaluate, prioritize, and manage multiple projects. Education
Bachelor's Degree in Engineering is Required Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Information Technology Industries: Software Development
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Systems Engineer - Assay Development with cytology specimens (Hybrid) Location: Tucson, AZ Duration: 12+ months Pay: $40.00/hr - $45.00/hr (base pay range) Responsibilities
Drive requirements definition, risk management, and verification & validation practices in projects. Define requirements, design system architectures, and implement solutions to meet IVD standards. Take ownership of project deliverables and facilitate decision-making with well-considered tradeoffs. Work cross-functionally with many stakeholders, balancing needs and tradeoffs to reach aligned outcomes. Qualifications
MUST HAVE
Requirement writing experience in a regulated industry (medical device industry preferred). Risk analysis (FMEA) experience in an engineering discipline (regulated medical device company preferred). Demonstrated knowledge of systems engineering principles, including requirements engineering, tradeoff analysis, risk management, configuration management, and verification & validation. Ability to work cross-functionally with many stakeholders and achieve alignment on needs and tradeoffs. IDEAL
Assay development experience, particularly with cytology specimens. Prior experience in RETINA (Requirements & Test Integration Application) and with LucidSpark/LucidChart. Excellent organizational skills with the ability to evaluate, prioritize, and manage multiple projects. Education
Bachelor's Degree in Engineering is Required Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Information Technology Industries: Software Development
#J-18808-Ljbffr