Jodi Murphy

About Jodi Murphy

High-performing, detail-oriented scientist with 25 years of experience working in an FDA and ISO regulated health care industry. Motivated by fast paced environments, and consistently delivers innovative results with integrity. Exceptional problem-solving, teamwork, technical writing, analytical, and communication skills. Significant experience in:• Project Management, 53 Projects Delivered On Time, Within Budget To-Date• Certified in BOK: Six Sigma Black Belt, Six Sigma Green Belt, and PMP• Software Validation, Boolean Logic, Data Mining, Software Life Cycle, and SAP ERP• ISO 13485:2016, ISO 9001:2015, 21 CFR 11, 21 CFR 820, and GPSV• IVD cGMP Small Scale Manufacturing• Abbott Commander, X-Systems, Cell-Dyn, ARCHITECT, PRISM, and Alinity s• Dilutions, Centrifugation, pH Adjustments, Gel Electrophoresis, and Southern Blotting• Business Process Owner for 7 Laboratory Data Management Systems (2015–2022)

Experience

1. Quality Program Manager, Change Management & Data Integrity

   Abbott

   Feb 2024 — Present · Lake County, IL, US

   Within Abbott Quality & Regulatory (AQR), act as the subject matter expert for data integrity, document management, change control, GDP, and personnel/training while also having a working knowledge of related Quality System elements (e.g, Medical Device Reporting, Nonconformance & CAPA, Design Controls, etc.). Seek to improve the effectiveness of the Abbott Quality System, including monitoring, trending, and analysis of Abbott compliance performance. Responsibilities are Abbottwide, covering all Abbott businesses/divisions, and include:• Leading global committees, teams, and communities of practice.• Providing direct business/division support and global consulting activities.• Participating in industry groups, conferences, and peer-sharing opportunities. • Acting as a change agent for incorporating best practice methods across the corporation.• Serving as a business/divisional liaison for AQR.• Managing multiple global projects impacting the overall Quality System, data integrity, change management, and personnel/training.• Maintaining oversight for confidential information across the project lifecycle.• Initiating significant interaction with executive management and accountability for assigned projects.

Education

• University of Cincinnati

  Bachelor of Science

• Kennesaw State University

  Master of Science

• DePaul University

  Master of Science

• University of Cincinnati

  Bachelor of Arts

Skills

• Change Control
• Leadership
• Quality Assurance
• Medical Devices
• Capa
• Data Analysis
• Technical Support
• Management
• Troubleshooting
• Cross-Functional Team Leadership
• Project Management
• Business Process Improvement
• Fda
• Training
• Testing
• U.s. Food and Drug Administration (Fda)
• Software Documentation
• Quality System
• Process Improvement
• Technical Writing
• Validation
• Gmp
• Analysis