Naveed Anjum
About Naveed Anjum
Naveed Anjum serves as the Quality Assurance Team Lead at Aimmune Therapeutics, where he has worked since 2019. He has extensive experience in quality assurance and validation roles across various pharmaceutical companies, including Gilead Sciences, Bayer HealthCare, and Pfizer.
Work at Aimmune Therapeutics
Naveed Anjum has been serving as the Quality Assurance Team Lead at Aimmune Therapeutics since 2019. In this role, he oversees quality assurance processes and ensures compliance with industry standards. His position is based in Brisbane, California, where he has contributed to the organization's commitment to delivering high-quality therapeutic solutions.
Previous Experience in Quality Assurance
Before joining Aimmune Therapeutics, Naveed Anjum held several positions in quality assurance and validation across various pharmaceutical companies. He worked at Gilead Sciences as a Data Integrity Specialist from 2021 to 2022. His earlier roles include Validation Site Lead at Bayer HealthCare and Validation Project Manager at Pfizer. These experiences provided him with a strong foundation in quality management and compliance.
Education and Expertise
Naveed Anjum studied at Osmania University, where he earned a degree in Engineering from 1991 to 1994. His educational background supports his extensive experience in quality assurance and validation within the pharmaceutical industry. He has developed expertise in implementing quality management systems and ensuring compliance with regulatory requirements.
Achievements in Quality Management
Throughout his career, Naveed Anjum has implemented several initiatives to enhance quality management processes. Notably, he implemented the eQMS SmartSolve System to improve document and change management. He also led the implementation of Compliance Wire Phase 2 to support the Enterprise Learning Management System, showcasing his commitment to advancing quality assurance practices.
Vendor Audits and Compliance
Naveed Anjum has conducted vendor audits for TraceLink and Scien Tek Software, ensuring compliance with GMP/FDA requirements. His role in supervising data migration from BioClinica CTMS to Veeva Vault CTMS highlights his attention to detail and commitment to maintaining high standards in quality assurance.