- Designed and reviewed new development for CMS's proposed 2024 Physician Fee Schedule Rule.- Coordinated customer communications and implementation of updates for the AMA's 2023 CPT code changes.- Subject matter expert for EpicCare Inpatient charging functionality experienced with the creation and implementation of physician charging best practices and professional charge automation processes to increase revenue and decrease costs at healthcare organizations.

- Reviewed 100+ issues for potential financial impact and published 20+ notifications to comply with regulatory requirements. - Coordinated customer notification and resolution of software issues with potential financial impact. - Led the review of application issues with potential financial risk via collaboration with subject matter experts to determine and scope and impact of issues. - Ensured processes for notification and fix implementations were documented and followed within expected time frames.

- Reviewed 100+ design documentation and code changes to ensure completion of development meeting quality standards.- Trained and certified software development proficiency for 25+ new team members using self-created training materials.- Communicated updates to development processes and expectations at 30+ monthly team meetings.

- Supported 50+ system go-lives, upgrades, and new functionality implementations across 20+ customer systems.- Developed 10+ MUMPS projects including ETL utilities for cleaning and managing large datasets and performance fixes. - Analyzed 1000+ error trace code stacks to determine source of crashes, performance slowdowns, and customer complains. - Packaged and delivered 20+ customer specific code bundles for deployment at customer systems using EMC2 CI/CD toolset.- Deployed 5 machine learning based models into live production systems using Epic’s Cognitive Computing Platform in collaboration with various Epic and customer data science experts and clinical subject matter experts. - Performed iterative improvements of predictive models using statistical analysis of validation runs on customer specific production data and clinical review from customer SMEs of inputs and outcomes.

- Followed laboratory SOPs to collect validation and verification data and to troubleshoot manufacturing issues– Validated and documented manufacturing process changes to ensure compliance with FDA and GLP standards– Safely produced chemical solutions using DEA controlled substances under heated conditions to test new agarose formulas– Setup molding presses, heat exchanges, and vacuum seal machines to improve efficiency in production laboratories