Sr Systems Engineer

Dawar Consulting, Inc.; Tucson (AZ); On-site; USD 62,000 - 83,000; Full time

Benefits offered by this job

Medical

Job summary

Dawar Consulting, Inc. in Tucson, AZ seeks a Sr Systems Engineer to support regulated life sciences programs. The role involves translating regulatory and stakeholder requirements into testable engineering specifications, and leading verification and validation activities.

You will develop TMV, DoE, test beds, and comprehensive test plans, while analyzing sensor data with Python and maintaining traceability using DOORS/RETINA/Jira. Experience in FDA/ISO environments is preferred.

Qualifications

• Bachelor's degree in Electrical, Chemical, Biomedical, Software Engineering, or a related discipline.
• Strong experience in systems engineering, testing, verification and validation, and requirements management.
• Proficiency in Python-based data analysis and troubleshooting.

Responsibilities

• Deliver V-Model systems engineering activities and participate in design reviews.
• Develop and execute Test Method Validation (TMV), test method development, and Design of Experiments (DoE).
• Develop test beds, testing protocols, and comprehensive verification and validation plans.
• Analyze digital sensor outputs and test data using Python and other analytical tools.
• Translate system, regulatory, safety, and stakeholder requirements into clear, testable engineering requirements.
• Establish and maintain requirements traceability using tools such as DOORS, RETINA, or Jira.
• Perform troubleshooting, investigate system defects, and evaluate performance against design specifications.
• Manage requirements, risk, configuration, verification, validation, and defect documentation.
• Prepare detailed technical reports and communicate findings to development partners.

Skills

Python

Data analysis

Requirements management

Education

Bachelor's degree in Electrical, Chemical, Biomedical, Software Engineering or related discipline

Tools

DOORS

RETINA

Jira

Job description

Tucson, United States | Posted on 11/13/2026

Our client, a world leader in biotechnology and life sciences, islooking for a“Sr Systems Engineer” based out of Tucson, AZ.

Job Duration:Long Term Contract(Possibility of Extension)

Pay Rate: $45/hr - $60/hr on W2

Company Benefits:

• Medical, Paid Sick leave(asper state policy)

Seeking a Systems Engineer to support systems engineering, test methoddevelopment, verification and validation, and design assurance activities in aregulated engineering environment. The role involves translating regulatory andstakeholder requirements into testable engineering specifications, developingtest plans, conducting hands-on testing, analyzing sensor data, and managingdefects throughout the product development lifecycle.

Key Responsibilities:

• Deliver V-Modelsystems engineering activities and participate in design reviews.
• Develop andexecute Test Method Validation (TMV), test method development, and Designof Experiments (DoE).
• Develop test beds,testing protocols, and comprehensive verification and validation plans.
• Analyze digitalsensor outputs and test data using Python and other analytical tools.
• Translate system,regulatory, safety, and stakeholder requirements into clear, testableengineering requirements.
• Establish andmaintain requirements traceability using tools such as DOORS, RETINA, orJira.
• Performtroubleshooting, investigate system defects, and evaluate performanceagainst design specifications.
• Managerequirements, risk, configuration, verification, validation, and defectdocumentation.
• Prepare detailedtechnical reports and communicate findings to development partners.

Required Qualifications:

• Bachelor's degreein Electrical, Chemical, Biomedical, Software Engineering, or a relateddiscipline.
• 4+ years ofexperience for Systems Engineer; 8+ years for Senior Systems Engineer.
• Strong experiencein systems engineering, testing, verification and validation, andrequirements management.
• Proficiency inPython-based data analysis and troubleshooting.
• Experienceinterpreting engineering specifications and translating them into testablerequirements.

Preferred Qualifications:

• Experience in FDA-or FAA-regulated environments, ideally medical devices.
• Knowledge of ISO,IEC, FDA and EU regulatory standards.
• Experience withV-Model systems engineering and requirements traceability.
• Familiarity withDOORS, RETINA, Jira, or similar requirements management tools.
• Experience withsensor testing, test method validation, DoE, and test bed development.