Software Engineer

Job Responsibilities:
- Design, implement, and maintain features/components across assigned clinical software applications; write testable, documented code for a regulated production environment.
- Deliver independently end-to-end (requirement refinement through release); surface risks/trade-offs early.
- Participate in design/architecture trade-off discussions.
- Perform and support peer code reviews; uphold code quality and compliance.
- Partner with product management to refine requirements, identify constraints, and estimate backlog items.
- Write and maintain automated unit, integration, and end-to-end tests.
- Produce technical documentation (design notes, ADRs, operational runbooks) meeting SOX and FDA change-control obligations.
- Instrument/monitor/support production systems; participate in incident response and root-cause analysis.
- Automate recurring manual tasks.
- Support newer engineers via code review and knowledge sharing.
- Use AI coding assistants and agentic workflows across design, implementation, and test generation (with peer/engineering review).

Required Qualifications:
- BS in CS/Software Engineering or related field (or equivalent experience).
- 2+ years professional software engineering in production systems.
- Full SDLC experience in a team environment (requirements, design, implementation, testing, release).
- Experience writing/maintaining automated tests for production.
- Routine peer code review practice.
- Regular use of modern AI-assisted development tooling.

Preferred Qualifications:
- Healthcare/clinical lab/diagnostics/life sciences software background.
- Agile delivery framework familiarity.
- Cloud-native development/deployment patterns.
- Experience in FDA/SOX/CLIA/HIPAA-governed environments.

Other:
- Periodic travel and on-call/after-hours support for production emergencies may be required.