Senior Systems Engineer

Seeking a hands-on Senior Systems Engineer with experience in electromechanical systems, system testing, and verification/validation, preferably within the medical device industry or an FDA/FAA-regulated environment. Develop test methods, test beds, and comprehensive testing plans; perform TMV, DOE, and hands-on system testing.

Our client, a world leader in biotechnology and life sciences, is looking for a “Senior Systems Engineer” based in Tucson, AZ.

 

Job Duration: Long Term Contract (Possibility of Extension)

Pay Rate: $50/hr - $60/hr on W2

 

Company Benefits: Medical, Paid Sick leave, 401K

 

Seeking a hands-on Senior Systems Engineer with experience in electromechanical systems, system testing, and verification/validation, preferably within the medical device industry or an FDA/FAA-regulated environment.

 

Key Responsibilities:

• Develop and execute system engineering deliverables following the V-Model and participate in design reviews.
  
• Develop test methods, test beds, and comprehensive testing plans; perform TMV, DOE, and hands-on system testing.
  
• Analyze sensor outputs and test data using Python and other data analysis techniques.
  
• Evaluate system performance against design specifications and troubleshoot system-level issues.
  
• Manage requirements, risk, configuration, verification/validation, and defect lifecycles using designated engineering tools.
  
• Author detailed technical reports and document test results, defects, and findings for development partners.
  
• Translate regulatory standards and stakeholder needs into clear, testable system, hardware, and software requirements.
  
• Maintain bidirectional traceability from regulations and requirements through design specifications and verification tests.
  

 

Required Qualifications:

• Bachelor’s degree in Electrical, Chemical, Biomedical, Software Engineering, or a related engineering field.
  
• Hands-on experience with electromechanical systems, test method development, troubleshooting, and system verification/validation.
  
• Python coding skills for data analysis.
  
• Experience with requirements management and traceability tools such as DOORS, Jira, or RETINA.
  

 

Preferred Qualifications

• Experience in the medical device industry or an FDA/FAA-regulated environment.
  
• Knowledge of ISO, IEC, FDA, and EU regulatory standards.
  
• Experience interpreting regulations and translating compliance requirements into system-level and lower-level engineering requirements.
  

 

If interested, please send us your updated resume at

hr@dawarconsulting.com

/

akansha@dawarconsulting.com