This role will be focused on implementing and supporting applications in the Quality and Regulatory (QRA) functional area within LRCGQ (Legal, Regulatory, Compliance, Government and Quality) GTBS (Global Technology Business Services) department.
Accountabilities in this role: Design and architect cloud-friendly applications using multiple cloud-based technologies. Design, implement and support integrations for SaaS solutions with various Cardinal Health applications. Build detailed design artifacts. Triage product support issues and assist in engaging the appropriate parties to resolve the issue in a timely manner. Work directly with business unit clients to understand business processes and elicit requirements. Lead, coordinate, and perform testing, verification, and validation of requirements. Maintain relationships with business associates in Quality and Regulatory departments. Maintain relationships with SaaS vendors. Practice Agile and DevSecOps methods in a geographically dispersed team. Qualifications: Bachelor's degree in related field or equivalent work experience. 5+ years of experience as a technology developer in a corporate environment. Programming and application development experience including one or more of the following technologies: JAVA, JAVA Spring Boot, Angular, Pivotal cloud foundry /Tanzu. Experience building microservices. Knowledge of database concepts and experience with database technology and SQL (e.g.: PostgreSQL). Experience in Agile and Hybrid methodologies. Proficiency in Microsoft Office products (Excel, Word, PowerPoint, etc.) and diagramming tools like Lucid Chart. Strong analytical, troubleshooting, and problem-solving skills. Excellent listening, communication, and presentation skills. Must be able to present and communicate technical concepts in a clear and concise manner to key leadership and stakeholders. Passionate/self-motivated for ongoing continuous learning. Additional Preferred Qualifications: Experience with EDA/streaming, ServiceNow, Jira, GitHub, Postman, Maven, Gradle. Familiarity with managing/solutioning applications in Cloud (GCP etc.). Prior experience working in an FDA validated environment supporting medical device quality or manufacturing is a plus.
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