Operations Manager for East Wing Manufacturing of the Catalent, St Petersburg facility. Transferred to East Wing to update to cGMP site requirements for Project Flamingo. Managed OTC/RX Environment. Streamlined improvement processes in East Wing to improve compliance and quality. Overseen the engineering updates to the wing to improve OEE and to limit downtime while meeting site shipping requirements.

Production Manager for HPAPI Manufacturing . Responsible for West Wing manufacturing area, focused on Rx and potent compounding (HPAPI) for world wide markets.Driving excellence in safety, quality, delivery, and cost in a patient first environment.100 direct and indirect reports executing shop floor manufacturing from Product Development to commercial manufacturing.First hand experience in QMS, cGMP, and Regulatory Compliance.

Train, Motivate and provide corrective actions to department associates. Responsible for daily operations in Med Prep, Gelatin Manufacturing, Encapsulation and Finished Product for packagingOversee blending of Active Pharmaceutical Ingredient (API) and other hazardous compounds. Ensure Compliance with established SOP’s and CFR211 for FDA approved manufacturing. Conduct Quality investigations and document deviation reports in order to determine disposition of discrepant product. Prepare Statistical data for process control and reporting

Launch of JD Edwards software for MRP/ERP within the production environment. Subject Matter Expert for Operations/Manufacturing and initiated real time executions for operations use. Successfully launched new program and currently act as the trainer for the operations portion within the system for the facility located in Clearwater, Florida.

Operations and Management, worked with Manufacturing supervisor and Production Manager to complete day-to-day operations within the softgel manufacturing process. Conduct Quality investigations and document deviation reports in order to determine disposition of discrepant product.

Train, Motivate and provide corrective actions to department associates. Responsible for daily operations in Med Prep, Gelatin Manufacturing, Encapsulation and Finished Product for packagingOversee blending of Active Pharmaceutical Ingredient (API) and other hazardous compounds. Ensure Compliance with established SOP’s and CFR211 for FDA approved manufacturing. Conduct Quality investigations and document deviation reports in order to determine disposition of discrepant product. Prepare Statistical data for process control and reporting

Assist in development of operators, a subject matter expert of multiple departments with the facility that are directly lined with the manufacturing process.

Responsible for up to 15+ associates depending on the average weekly sales of specific retail outlets. Work side by side with other department managers and upper management to escalate weekly sales in cross merchandising. Followed and prepared Product Management Guides (PMG’s) in order to reduce the cost of rejected raw materials, and finished goods. Responsible for daily operations for planning and setup for the next work day. Proficient in meeting timely deadlines for customer base orders. Maintained above standards for cleanliness and compliance of state and local laws and regulation for the Florida Department of Agriculture. Interviewed, Hired and Terminated within policy guidelines. Trained for further development within the organization.