José L Velázquez
About José L Velázquez
José L Velázquez is a Senior Chemist with extensive experience in the pharmaceutical industry, currently working at QuVa Pharma, Inc. since 2018. He has a strong background in pharmaceutical instrumentation and has held various roles at notable companies including Akorn Pharmaceutical and Catalent Pharma Solutions.
Work at QuVa Pharma
José L Velázquez has been employed at QuVa Pharma, Inc. as a Senior Chemist since 2018. His role involves conducting Particle Matter tests for all vial and syringe products. He applies his extensive knowledge in pharmaceutical instrumentation and dissolution method development to ensure compliance with current Good Manufacturing Practices (GMP), International Council for Harmonisation (ICH) guidelines, and United States Pharmacopeia (USP) tests. His contributions have been significant in maintaining the quality and safety of pharmaceutical products.
Previous Experience in Pharmaceuticals
Before joining QuVa Pharma, José L Velázquez gained diverse experience in the pharmaceutical industry. He worked at Akorn Pharmaceutical as a Chemist from 2016 to 2018, where he further developed his skills in Somerset County, New Jersey. His earlier roles include Formulation Chemist at Faulding Pharmaceuticals from 1995 to 1997, Process Chemist at Par Pharmaceutical for six months in 2018, and R&D Scientist at Catalent Pharma Solutions from 2007 to 2015. These positions provided him with a broad foundation in various aspects of pharmaceutical development and quality control.
Education and Expertise
José L Velázquez studied at the Interamerican University of Puerto Rico, where he earned a Bachelor of Applied Science (B.A.Sc.) in Chemistry from 1978 to 1983. His educational background laid the groundwork for his extensive expertise in pharmaceutical instrumentation, particularly with Ultra Performance Liquid Chromatography (UPLC) systems and Empower 3 software for documentation and reporting. This knowledge has been pivotal in his roles throughout his career.
Background in Chemical Analysis
José L Velázquez has a long history in chemical analysis within the pharmaceutical sector. His career began at DuPont Pharmaceuticals as a Chemical Technician from 1989 to 1995, followed by a position as a QC Chemist at URL Pharma, Inc. from 1997 to 2000. He also worked as an R&D Chemist at Bio-Pharm Inc. from 2015 to 2016. His background includes a strong emphasis on quality assurance and method development, which has been essential in his subsequent roles.
Professional Skills and Contributions
Throughout his career, José L Velázquez has demonstrated a strong ability to coordinate efforts in a quality work environment. His skills in dissolution method development and adherence to regulatory guidelines have contributed to successful product outcomes. His experience with UPLC systems and conducting Particle Matter tests showcases his technical proficiency and commitment to maintaining high standards in pharmaceutical development.