Our Client, an American Biotechnology company, is looking for a Software Engineer (Systems) 4 for their Santa Clara, CA/Hybrid location.
Responsibilities:
• Support the design, implementation, and sustainment of CI/CD pipelines with embedded with auditable deployment processes.
• Promote infrastructure-as-code using Terraform, Helm, and Ansible, incorporating HITRUST and GxP controls into reusable modules.
• Architect and maintain highly available, scalable, and compliant systems leveraging Kubernetes and cloud platforms (AWS, GCP, Azure).
• Apply SRE principles—defining, measuring, and improving reliability metrics (SLIs/SLOs/SLAs) in regulated healthcare environments.
• Lead capacity planning, performance tuning, and infrastructure optimization initiatives focused on regulatory and privacy requirements.
• Manage the full incident lifecycle (detection, triage, resolution, postmortem), documenting as required for FDA compliance and audit readiness.
• Develop and maintain incident response playbooks, including IT and regulatory escalation protocols.
• Implement and manage monitoring solutions (Datadog, Prometheus, Grafana, Elastic Search) to support rapid issue identification in compliance with healthcare mandates.
• Integrate and manage SIEM tools (Splunk, Datadog Security, Elastic Security) for log aggregation, threat detection, and support of regulatory audits (HITRUST, GxP).
• Collaborate with security, quality assurance, and regulatory teams to monitor and respond to production security incidents.
• Ensure logging, auditing, and reporting meet FDA, HITRUST, ISO 27001 and healthcare industry standards—including data retention, traceability, and privacy safeguards.
• Document and communicate infrastructure processes clearly to facilitate internal knowledge transfer and external audit readiness.
• Plan and manage resource utilization to meet both performance goals and regulatory efficiency standards.
• Troubleshoot and support cloud/network issues, ensuring secure handling of protected health information (PHI) and device data.
Requirements:
• Bachelor’s or Master’s degree in Computer Science, Engineering, or related field.
• 7+ years in Site Reliability Engineering, DevOps roles within healthcare, medical device, or life sciences industries.
• Expertise in containerization (Kubernetes, Docker), cloud platforms, and infrastructure-as-code.
• Direct experience supporting systems subject to FDA GxP and HITRUST compliance; familiarity with HIPAA, SOC2, ISO 27001 frameworks.
• Strong skills in scripting/automation (Python, Bash, Go).
• Proven track record managing SIEM and monitoring platforms in regulated environments.
• In-depth knowledge of incident response and reliability engineering in healthcare/medical device settings.
• Certifications in cloud security, DevOps, and/or healthcare compliance (e.g., HITRUST, AWS Security, etc.) strongly preferred.
• Preferred Skills:
• Experience deploying and supporting medical device software under FDA regulations.
• Familiarity with quality management systems, validation procedures, and documentation for regulatory audits and FDA submissions.
• Strong communication and leadership skills for cross-functional collaboration in a regulated setting.
• Ability to innovate while maintaining strict compliance constraints.
Why Should You Apply?
• Health Benefits
• Referral Program
• Excellent growth and advancement opportunities