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Nesco Resource · 17 hours ago

Systems Engineer - Lotus Project

Tucson, AZ

Full-time

Onsite

Mid Level

$42/hr - $45/hr

4+ years exp

Nesco Resource is seeking a motivated Systems Engineer for their Tissue Diagnostics division to drive product definition and system architecture design. This role focuses on advancing cancer diagnostics through automation and requires collaboration with various teams to meet IVD standards.

ConsultingHuman ResourcesStaffing Agency

Responsibilities

System Lifecycle Management: Apply Systems Engineering to product definition, requirements, risk analysis, and testing

Project Execution: Manage requirements, risk analysis, and verification/validation

Industry and Technology Analysis: Research trends, emerging technologies, and competitive products' differentiation

Cross-functional Collaboration: Work with R&D, Marketing, Operations, Quality, and Regulatory teams to ensure alignment

Customer-Focused Innovation: Engage with business leaders and VoC representatives to align technical solutions with customer needs

Technical Problem Solving: Analyze complex technical challenges, present solutions, and facilitate informed decision-making

Qualification

Systems EngineeringRequirements EngineeringRisk ManagementElectro-mechanical DevicesRegulated Medical Device ExperienceCollaboration SkillsCommunication SkillsOrganizational Skills

Required

Experience in front-end Systems Engineering design & development deliverables around requirements, risks & architecture

Ability to work independently and cross-functionally with many different groups to solicit needs and complete trade off analyses

Experience in a regulated medical device industry

Bachelor's degree in Engineering, Biomedical Sciences, or related technical field with 4 years of experience (or Master's with 2 years, or PhD)

Demonstrated knowledge in systems and hardware integration and testing, including requirements engineering, tradeoff analysis, risk management, and verification/validation using tools like RETINA

Experience in a regulated environment, familiar with FDA, ISO, and other relevant diagnostic product standards

Interest in innovative technologies and understanding of the IVD competitive landscape