Cheryl L Benton, 77New York, NY

Greater New York City Area

Marketing and Advertising

United States

United States

Novartis Pharmaceutical Jan 2008 to Present
Associate Scientist Union County College - Cranford, NJ Nov 2007 to Apr 2008
Pharmaceutical Technician, Completed State Certified Merck Jun 1986 to May 2007
Stability Coordinator

Halo Pharma - Whippany, NJ Apr 2013 to May 2014
Stability Supervisor Novartis Pharmaceutical - East Hanover, NJ Jan 2008 to Mar 2013
Associate Scientist - Stability Expertise Merck Jun 1986 to May 2007
Stability Coordinator

Union County College - Cranford, NJ Nov 2007 to Apr 2008
Pharmacy Technician Certified Essex County College - Newark, NJ Feb 1986 to Jun 1986

Professional with over twenty years of experience in the Pharmaceutical Industry with expertise in Quality Assurance Clinical, Research Stability. Supervisor the monitoring team and study sites with relevant study information, and supporting clinical operations and third party documents. Responsible for stability protocols, stability plans, stability reports and other stability documents, in alignment with established procedures and using LIMS templates. Supervisor Stability department and laboratory contract company Organizes readiness for and participate during regulatory inspections (FDA, EMA and DEA) and internal audits. Supervisor and support the development of SOP and Cgmp guidelines related to production planning and scheduling inventory management. Handling international distribution, transportation, disposition of stability phase I thru IV Project for QC and Clinical research department. Interpersonal skills with the ability to work in a team oriented environment, including cross-functional Project Teams involving members from Marketing, Supply, Manufacturing as well as R&D and Quality Control. Supervisor 5 or more employee in developing overall clinical plans and study protocols Stability and Laboratory Division. Customer service driven and leadership in Pharmaceutical and Contract Laboratory setting. For stability Project and Environmental Chamber Control for Quality Control /Product Development Department. Demonstrated success in organization of pulling samples and label printing for analytical testing for OTC final products; plus offsite and onsite testing on samples required per LIMS Protocol Freeze-Thaw Studies and Photo Stability Studies In-Use-Test. I thrive in challenging and results oriented environments and it is these qualities that attract me to a career with a company such as yours. As a highly motivated individual, I have a strong desire to exceed expectations and deliver the effort necessary to achieve company goals. I would welcome the opportunity to discuss how I can fill the needs of this position. In the interim, I thank you for reviewing this letter and the accompanying material.