Systems Engineer - Software

Job Title: Systems Engineer – Software Requirements & Risk
Location: 1910 East Innovation Park Drive, Tucson, AZ
Duration: 10-month contract (potential for extension or permanent hire)
Pay Rate: $42–$45/hour (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage

Position Overview
Roche Tissue Diagnostics is seeking a Systems Engineer to lead software product definition and development across system architecture, requirements engineering, and risk analysis. This position plays a vital role in shaping next-generation cancer diagnostic instruments and automation solutions used worldwide in over 250 cancer tests.

Key Responsibilities

• System Lifecycle Management:
  Apply Systems Engineering principles to define software requirements, perform risk assessments, and ensure compliance through verification and validation activities.
• Project Execution:
  Manage all aspects of software requirements, configuration, defect tracking, and testing deliverables in accordance with IVD standards.
• Cross-Functional Collaboration:
  Partner closely with R&D, Quality, Regulatory, Marketing, and Operations teams to align product requirements and ensure design integrity.
• Innovation & Research:
  Evaluate emerging technologies, industry trends, and competitive offerings to support continuous product innovation and differentiation.
• Customer Focus:
  Collaborate with business leaders and Voice of Customer (VoC) teams to translate user needs into robust technical solutions.
• Technical Problem Solving:
  Identify and resolve complex technical challenges through analytical approaches and structured decision-making.

Qualifications
Education:

• Bachelor's degree in Engineering, Biomedical Sciences, or a related technical discipline with 4+ years of experience,
  or a Master's degree with 2+ years,
  or a PhD in a relevant field.

Required Experience & Skills:

• Proven expertise in software requirements engineering, risk management, configuration management, and system verification/validation.
• Ability to work independently and collaboratively across diverse functional teams.
• Strong analytical and problem-solving skills with attention to detail.
• Experience in a regulated medical device or IVD industry, familiar with FDA and ISO standards.

Preferred Qualifications:

• Proficiency in software reliability, usability, and manufacturability principles.
• Excellent communication, leadership, and organizational skills.
• Ability to prioritize and manage multiple projects in a fast-paced environment.
• Demonstrated interest in emerging technologies and innovation in diagnostics.