Haris Panjwani
About Haris Panjwani
Haris Panjwani is a Quality Assurance Specialist at QuVa Pharma, Inc. in Houston, Texas, where he ensures compliance with GMP and cGMP standards and has improved production efficiency by 10%.
Work at QuVa Pharma
Haris Panjwani has been employed at QuVa Pharma, Inc. as a Quality Assurance Specialist since 2021. In this role, he focuses on ensuring compliance with Good Manufacturing Practices (GMP) and current Good Manufacturing Practices (cGMP) standards. His responsibilities include identifying process deviations in various stages of production, such as compounding, post-compounding, labeling, and inspection activities. He is based in Houston, Texas, and has contributed to the company's commitment to quality and regulatory compliance.
Education and Expertise
Haris Panjwani studied at ITT Technical Institute, where he pursued a degree in Computer Engineering. He completed his Associates of Computer Science from 2009 to 2011. This educational background provides him with a solid foundation in technical principles, which he applies in his role in quality assurance within the pharmaceutical industry.
Quality Assurance Responsibilities
In his capacity as a Quality Assurance Specialist, Haris Panjwani performs environmental monitoring in aseptic environments. This includes conducting viable air and non-viable particulate counts to ensure that the manufacturing environment meets stringent quality standards. His work is critical in maintaining the integrity of the production process and ensuring product safety.
Achievements in Production Efficiency
Haris Panjwani has successfully improved production efficiency by 10% through the implementation of process investigation reports. His analytical skills and attention to detail have contributed to optimizing production processes, thereby enhancing overall operational performance at QuVa Pharma.