Job description

Our Client, a Biotech company, is looking for a Senior Systems Engineer for their Tucson, AZ location. Responsibilities: • TMV, Test Method Development, DoE, data analysis (python coding capability) • Digital outputs of a sensor and analyze the data • Test bed development • Troubleshooting skills • Developing comprehensive testing plans. • Executing hands-on testing protocols. • Authoring detailed technical reports. • Managing the defect lifecycle (collection, documentation, and summarization for our development partner). Requirements: • Has expertise in translating industry standards, government regulations, and high-level stakeholder mandates into clear, testable engineering requirements. • Has experience and ability to read, interpret, and trace legal, safety, and industry regulations (e.g., ISO, IEC, FDA, EU standards) without losing intent. • Has experience in extracting functional, performance, interface, and constraint requirements from dense regulatory text and ambiguous stakeholder inputs. • Has experience breaking down high-level "shall" statements or compliance mandates into lower-level requirements for hardware, software, and system. • Has experience establishing bi-directional traceability (e.g., using tools like RETINA, DOORS, or Jira) linking source regulations → system requirements → design specifications → verification tests • Education & experience: • Degree: Bachelor’s degree in engineering (Electrical, Chemical, Biomedical, or Software preferred) • Years of Experience: 8 yrs • Experience in a FDA or FAA regulated environment is a strong plus; Medical device industry is ideal Why Should You Apply? • Health Benefits • Referral Program • Excellent growth and advancement opportunities

Requirements

Must-haves

Our Client, a Biotech company, is looking for a Senior Systems Engineer for their Tucson, AZ location.
TMV, Test Method Development, DoE, data analysis (python coding capability)
Digital outputs of a sensor and analyze the data
Test bed development
Troubleshooting skills
Developing comprehensive testing plans.
Executing hands-on testing protocols.
Authoring detailed technical reports.
Managing the defect lifecycle (collection, documentation, and summarization for our development partner).
Has expertise in translating industry standards, government regulations, and high-level stakeholder mandates into clear, testable engineering requirements.
Has experience and ability to read, interpret, and trace legal, safety, and industry regulations (e.g., ISO, IEC, FDA, EU standards) without losing intent.
Has experience in extracting functional, performance, interface, and constraint requirements from dense regulatory text and ambiguous stakeholder inputs.
Has experience breaking down high-level "shall" statements or compliance mandates into lower-level requirements for hardware, software, and system.
Has experience establishing bi-directional traceability (e.g., using tools like RETINA, DOORS, or Jira) linking source regulations → system requirements → design specifications → verification tests
Years of Experience: 8 yrs
Experience in a FDA or FAA regulated environment is a strong plus; Medical device industry is ideal
Why Should You Apply?
Referral Program
Excellent growth and advancement opportunities

Nice-to-haves

Degree: Bachelor’s degree in engineering (Electrical, Chemical, Biomedical, or Software preferred)

Application prep

Use the role’s language and application details while tailoring your materials.

Keywords to mirror

pythonjira

Platform: jobdiva
Effort: medium