David Jimenez
About David Jimenez
David Jimenez serves as the Manufacturing ILP Supervisor at QuVa Pharma, Inc., where he has worked since 2021. He has extensive experience in regulated environments and has held various supervisory roles at AmerisourceBergen since 2006.
Work at QuVa Pharma
David Jimenez has been serving as the Manufacturing ILP Supervisor at QuVa Pharma since 2021. In this role, he oversees manufacturing processes and ensures compliance with industry regulations. His responsibilities include managing production schedules, maintaining quality standards, and leading a team to achieve operational goals. His tenure at QuVa Pharma has contributed to the company's commitment to delivering high-quality pharmaceutical products.
Experience at AmerisourceBergen
David Jimenez has worked at AmerisourceBergen since 2006, holding the position of Operations and Clean Room Supervisor. With 18 years of experience in this role, he is responsible for supervising clean room operations and ensuring adherence to safety and quality protocols. His extensive experience in a regulated environment has equipped him with the skills necessary to manage complex operational challenges effectively.
Career Background
David Jimenez began his career at Texas Instruments as a Semiconductor Chip Test Operator from 2000 to 2006. He progressed through various positions, including Order Selector, Sanitizer Technician, Lead Production Technician, and Pharmacy Technician, before advancing to supervisory roles. This diverse background has provided him with a comprehensive understanding of manufacturing and operational processes within the pharmaceutical industry.
Education and Qualifications
David Jimenez studied at Medvance Institute-Houston, where he achieved certification as a Pharmacy Technician IV. He also attended Houston Community College, earning an Applied Science degree. His educational background supports his expertise in pharmaceutical manufacturing and regulatory compliance, enhancing his ability to contribute to project and company objectives.
Regulatory Experience
David Jimenez possesses over 13 years of experience working in regulated environments, specifically in USP 797 Pharmaceutical and 503B Sterile to Sterile Preparations compounding manufacturing facilities. His knowledge of regulatory standards and practices is essential for maintaining compliance and ensuring the safety and efficacy of pharmaceutical products.