Ji-Ang Liu

Ji-Ang Liu serves as the Senior Manager of Analytical Development and Quality Control at Aspire Pharmaceuticals, where he plays a pivotal role in ensuring the integrity and compliance of pharmaceutical products throughout their lifecycle. With a robust background in biotechnology and drug development, Ji-Ang expertly manages the release of raw materials, in-process samples, and finished products, all while adhering to stringent Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). His leadership extends to overseeing a dedicated analytical team, where he fosters a collaborative environment to tackle complex analytical challenges and drive innovative solutions.

At Aspire Pharmaceuticals, Ji-Ang is instrumental in method development, verification, validation, and transfer, ensuring that all analytical methodologies meet the rigorous standards required for regulatory filings. He is also responsible for executing stability studies and product release operations, which are critical for maintaining product quality and compliance. His keen oversight of departmental budgets and resource allocation ensures that the analytical team operates efficiently while delivering high-quality results.

Ji-Ang’s expertise in High-Performance Liquid Chromatography (HPLC) and other analytical techniques enables him to review and approve test methods, specifications, and Certificates of Analysis (CoA), ensuring that all outputs align with regulatory expectations. He actively engages in lab investigations and manages deviations, demonstrating his commitment to continuous improvement and quality assurance. Ji-Ang also plays a crucial role in preparing for FDA and other regulatory inspections, showcasing his deep understanding of compliance requirements in the life sciences sector. Through his strategic leadership and technical acumen, Ji-Ang Liu significantly contributes to Aspire Pharmaceuticals' mission of delivering safe and effective therapeutic solutions to patients.