Kimberly Babcock
Vendor Operations Lead for Novartis @IQVIA
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WORK HISTORY
Vendor Operations Lead for Novartis @IQVIA
US
Participate and manage project teams to support continuous improvement initiatives and other leadership team initiatives.• Coordinate the creation of standards with support of VPG team members• Facilitate workshops to enable and drive participants to create first in class process operating models to enhance communication across departments and decrease duplication of work.• Represent the VPG group to review and contribute to processes in other GDO units which impact supplier operations.• Manage Business Continuity Program across vendors within VPG.• Build SharePoint site to support departmental storage of resources, documents, and updates.• Creation of TMF Mapping Tool to support Clinical Trial Team across categories.• Creation of KBP Dashboard to support updates to Executive management.
EDUCATION
University of Maryland Global Campus
On-line Courses in Biotechnology Master’s Program
North Carolina Wesleyan University
Bachelor of Science, Biology, General
North Carolina Wesleyan University
BS, Biology
UMUC
Courses in Microbiology and Bioinformatics, Biotechnology
SKILLS
ABOUT KIMBERLY BABCOCK
Biotechnology professional, with experience in multiple disciplines of the industry: Stability Study Management, Analytical and QC Program Management and QC Sampling Design, Planning / Purchasing of Raw Materials and Consumables, including Project Cost Analysis; Project Improvement Initiatives, SharePoint Design; Experience using SAP, PAS-X, MS Project, Excel Pivots, Visio, PowerPoint, JUMP, Minitab, LIMS, SharePoint, Qlik, Power Automate.Achievements Include: Cost saving initiatives included eliminating endotoxin testing of all plant water stills; eliminated Pyrogen testing and converted all product endotoxin analysis to LAL testing. Received 2004 President\'s Achieving Excellence Award by identifying major trends in stability and manufacturing data of all 7 serotypes for Prevnar. Transferred all Wyeth Pearl River, NY Stability Studies to Wyeth RTP, NC. Managed 3 to 4 projects at a time, supporting Analytical / QC assay development and sampling plans and 3rd-party testing. Transferred inventory and setup projects into SAP within a 6-month timeframe without manufacturing shutdown. Creation of a Vendor Management Tool to support eTMF filing across multiple vendor alliances Implemented KPI Dashboard to provide updates to Leadership Team on Progression of Clinical Trials Built SharePoint site to support Novartis Vendor Partnership and Governance.
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