The Accounting Systems & Data Integration Analyst supports Axos Bank's Accounting & Finance initiatives, with primary focus on Jack Henry SilverLake, Enterprise Workflow (EWF), and Loan IQ platforms. The role designs, develops, and maintains integrations between banking systems and Finance applications, manages transaction-to-GL mapping, performs data validation and reconciliation, and ensures accounting data integrity across lending, deposit, treasury, and operations. Responsibilities include requirements gathering, interface development, testing, production support, SOX/audit compliance coordination, and leveraging AI tools (Copilot, Claude) to accelerate requirements analysis, testing, and automation. The position requires 10+ years of experience in system integrations and data interfaces within banking or financial services, with strong expertise in Jack Henry platforms, Azure DevOps, ServiceNow, SQL, APIs, and file-based integrations.
Software Gigs
The HTM Cybersecurity Program Manager leads cybersecurity and clinical technology programs at a healthcare system, managing a team responsible for diagnostic imaging and therapeutic equipment maintenance, regulatory compliance, and incident response. The role requires directing staff performance, managing budgets and procurement, and ensuring HIPAA and Joint Commission compliance while mentoring technical teams. Key responsibilities include risk assessment, cybersecurity strategy implementation, audit readiness, and collaboration with clinical teams to resolve technology issues affecting patient care. The ideal candidate brings 3+ years of management experience, 5+ years in healthcare technology operations, and deep knowledge of healthcare regulatory frameworks.
Senior Software QA Engineer supporting Dexcom's Postmarket Investigations team to assess real-world product performance, investigate software and device issues, and drive continuous improvement. You will collaborate across R&D, Quality, Regulatory Affairs, and Clinical teams to conduct root-cause analyses, perform risk assessments (including hazard analysis, DFMEA, PFMEA), and translate postmarket insights into product enhancements. The role requires deep technical understanding of software architecture, structured problem-solving, statistical analysis, and the ability to communicate findings to both technical and non-technical stakeholders while ensuring regulatory compliance and patient safety.
The Quality Assurance Specialist II independently owns and operates defined Quality Management System processes, serving as a subject matter expert for batch release, NCMR/deviation/CAPA management, and asset control. The role requires judicious decision-making on routine and moderately complex quality and compliance matters, including investigating quality events, driving corrective actions, and supporting regulatory submissions and FDA inspections. The specialist works collaboratively with a QA Associate and Sr. Quality Systems Engineer, leading process improvements and providing escalation support with minimal oversight.
Lead compliance testing and product certification for a portfolio of medical devices, including developing test strategies, managing external laboratories and certification bodies, and ensuring products meet safety, EMC, wireless, and regulatory requirements. Oversee compliance documentation, support design reviews and risk management, and monitor evolving regulatory standards. Manage a team of compliance engineers, departmental budgets, and drive process improvements in testing efficiency. Requires 5–8+ years of medical device compliance/certification experience and a technical degree (Mechanical, Electrical, or Biomedical Engineering).
Lead enterprise-level Clinical Data Management function across a biopharmaceutical company's clinical development portfolio. Establish CDM strategy, governance framework, operating model, and capability roadmap while ensuring accurate, complete, timely, inspection-ready clinical trial data. Drive data quality, risk management, database readiness, and cross-functional collaboration with biostatistics, statistical programming, and CRO/vendor partners. Oversee the clinical data lifecycle from protocol and CRF design through SDTM-ready analysis data.