Senior Systems Engineer: Onsite Electro-Mechanical Testing

Planet Pharma

Tucson (AZ)

On-site

USD 69,000 - 83,000

Full time

4 hours ago
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Job summary

Planet Pharma in Tucson, AZ is seeking a motivated Systems Engineer or Senior Systems Engineer for an onsite role concentrating on electro-mechanical devices. You will deliver V-Model systems engineering outputs, conduct development and testing, and ensure assays operate efficiently using the latest technologies and systems.

The ideal candidate has experience translating regulations into clear engineering requirements, can interpret ISO/IEC FDA/EU standards, and will contribute to traceability

Qualifications

  • Bachelor's degree in Engineering (Electrical, Chemical, Biomedical or Software preferred).
  • 4+ years for Systems Engineer level; 8+ years for Senior Systems Engineer level.
  • Experience in FDA or FAA regulated environments is a strong plus; Medical device industry is ideal.
  • Ability to translate regulations into testable requirements and traceability.

Responsibilities

  • TMV, Test Method Development, DoE, data analysis.
  • Digital outputs of a sensor and analyze the data.
  • Test bed development.
  • Troubleshooting skills and hands-on testing protocols.
  • Developing comprehensive testing plans.
  • Executing hands-on testing protocols.
  • Authoring detailed technical reports.
  • Managing the defect lifecycle with development partner.

Skills

Test Method Development
Design of Experiments (DoE)
Python scripting
Sensor data analysis
Test bed development
Troubleshooting
Testing plans
Hands-on testing
Technical reporting
Defect lifecycle management

Education

Bachelor's degree in Engineering

Tools

RETINA
DOORS
Jira

Job description

Planet Pharma in Tucson, AZ is seeking a motivated Systems Engineer or Senior Systems Engineer for an onsite role concentrating on electro-mechanical devices. You will deliver V-Model systems engineering outputs, conduct development and testing, and ensure assays operate efficiently using the latest technologies and systems.

The ideal candidate has experience translating regulations into clear engineering requirements, can interpret ISO/IEC FDA/EU standards, and will contribute to traceability

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