Dr. Samir Handal

Managed the company's pharmaceutical carton manufacturing facility. Managed site Documentation Group performing creation, revision and review of master production records and Managed site training activities. Wrote, revised, reviewed and approved standard operating procedures, change controls, deviations and investigations. Performed vendor audits. Delivered record of achievements both in leadership and laboratory technicalities. Likewise,

Continually looks for opportunities both conventional and creative way to contribute to the bottom line and in identifying and capturing market opportunities to accelerate expansion, increase revenue, and improve profit contributions in highly competitive industries.

Performed and authored investigations and developed appropriate corrective and preventive action plans. Hosted customer and regulatory audits. Interfaced with all organizational levels to ensure company compliance and company Standard Operating Procedures.

Managed quality of company's pharmaceutical carton manufacturing facility. Managed site Documentation Group performing creation, revision and review of master production records and completed records. Managed site training activities.

Responsible for building robust quality and operations organizations in the company, updating systems, practices and procedures to most recent standards and driving production efficiencies, defect reduction and process improvements leading to improved department and company performance and increased customer satisfaction.

Contributed to the identification of the CDK clinical candidate and to the success of the project. His enthusiasm and commitment were remarkable and my interactions with Xin-Jie on this project are one of the most memorable and productive during my time in preclinical research.