Our client, a world leader in biotechnology and life sciences, is looking 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(as per state policy)
Seeking a Systems Engineer to support systems engineering, test method development, verification and validation, and design assurance activities in a regulated engineering environment. The role involves translating regulatory and stakeholder requirements into testable engineering specifications, developing test plans, conducting hands-on testing, analyzing sensor data, and managing defects throughout the product development lifecycle.
Key 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.
Required Qualifications:
- Bachelor's degree in Electrical, Chemical, Biomedical, Software Engineering, or a related discipline.
- 4+ years of experience for Systems Engineer; 8+ years for Senior Systems Engineer.
- Strong experience in systems engineering, testing, verification and validation, and requirements management.
- Proficiency in Python-based data analysis and troubleshooting.
- Experience interpreting engineering specifications and translating them into testable requirements.
Preferred Qualifications:
- Experience in FDA- or FAA-regulated environments, ideally medical devices.
- Knowledge of ISO, IEC, FDA and EU regulatory standards.
- Experience with V-Model systems engineering and requirements traceability.
- Familiarity with DOORS, RETINA, Jira, or similar requirements management tools.
- Experience with sensor testing, test method validation, DoE, and test bed development.
If interested, please send us your updated resume at
hr@dawarconsulting.com
/
akansha@dawarconsulting.com