Jobs · Engineering · California

Software Engineer

On-siteEngineering$110–$140/hrContract

Location: San Diego, CA • Onsite • Contract (Temp-to-Hire) • 10 months

About the role

Design, develop, and test software on multiple instrumentation platforms (Panther System, Panther Fusion System) and a menu of assays (Aptima STIs, Aptima Virology, Panther Fusion Respiratory) for automated molecular diagnostic instruments.

Responsibilities

  • Design, develop, and test software for automated molecular diagnostic instruments.
  • Support Panther System and Panther Fusion System software platforms.
  • Participate in sprint planning and software work breakdown activities.
  • Develop software requirements and specifications.
  • Enhance existing applications through refactoring.
  • Perform code reviews.
  • Conduct unit and acceptance testing.
  • Perform root cause analysis and defect resolution.
  • Create and maintain technical documentation.

Requirements

  • BS or MS degree in Computer Science or equivalent.
  • C# .NET and object-oriented programming experience.
  • Experience with the Software Development Life Cycle (SDLC).
  • Strong analytical and problem-solving skills.
  • Experience working within structured development environments.
  • Applicants must be authorized to work for ANY employer in the U.S. (no visa sponsorship available).

Preferred Qualifications

  • 3–5 years of software development experience.
  • WPF (Windows Presentation Foundation).
  • AI knowledge/exposure.
  • Experience using AI-assisted development tools such as GitHub Copilot, Claude, or similar.
  • Agile/Scrum experience.

Pay

$110.00–$140.00 / hour (USD)

Schedule

Standard first shift, Monday–Friday

Benefits

  • Medical, vision, and dental insurance plans.
  • 401k retirement fund.

About the Client

This client operates in the medical device manufacturing industry, developing automated molecular diagnostic instruments and assays with a strong emphasis on women's health and diagnostic technology. The organization works within an FDA-regulated environment requiring strict adherence to GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).

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