• Plan, direct and administer the production activities for 2 business sites • Plan, direct and administer the distribution and receiving activities for 3 business sites• Use the MAS500 ERP system to control inventory, purchasing and distribution functions for 2 business sites• Provide human resource management for staff on 2 business sites• Prepare for and participate in ISO 9001:2008 audits for 2 business sites• Investigate and prepare reports for Non-Conformance Issues and Corrective Actions• Identify and implement cost saving measures based on business and budget objectives

• Review, validate, track and file international clinical trial study documents• Quality check drug safety reports used for regulatory submissions• Assist with the logistical aspect of the Serious Adverse Events reports received by participating trial sites

• Hired as GMP Manufacturing Operator for the contract manufacturing of the Active Pharmaceutical Ingredient (API) for Macugen. Duties included manufacturing intermediates and APIs in accordance with GMP requirements, completing equipment installation, operational and performance qualifications, validating manufacturing processes, handling chemicals, operating large and small-scale laboratory equipment, conducting preventative maintenance and trouble shooting both the equipment and process.• Promoted to GMP Alternate Shift Supervisor in 2004 and then GMP Shift Supervisor in 2005, additional duties included overseeing the shift performance based manufacturing scheduling, conducting operator training and performance reviews, investigating deviations and implementing corrective and preventative actions, inter-departmental activity coordination, as well as writing and reviewing SOPs and batch records.• Promoted to GMP Operations Supervisor in 2008, additional duties included overseeing raw material sourcing and receiving, performing vendor qualifications, creating and maintaining production schedules, writing quality based reports such as Annual Product Reviews, deviation reports, and HSE regulatory reports, maintaining HSE reporting database, coordinating and completing intermediate, API and sample shipments, liaising with the client to ensure smooth technology transfer during decommissioning, decommissioning manufacturing unit.