Lorey Trier
About Lorey Trier
Lorey Trier is a seasoned professional in quality assurance and compliance, currently serving as Associate Director of Quality at Neogene Therapeutics. With over 20 years of experience in the biotechnology industry, Trier has a strong background in GxP standards and ISO 13485 compliance.
Work at Neogene Therapeutics
Lorey Trier has been serving as the Associate Director of Quality at Neogene Therapeutics since 2021. In this role, she focuses on implementing and maintaining Good Practice (GxP) standards and ensuring compliance with ISO 13485. Her responsibilities include overseeing quality assurance processes and leading initiatives that enhance the overall quality system within the organization. Neogene Therapeutics is located in Santa Monica, California, where Trier has contributed to the company's commitment to quality in the biotechnology sector.
Work at Kite Pharma
Since 2017, Lorey Trier has held the position of Sr. Manager Compliance, Quality System Documentation at Kite Pharma. In this capacity, she has been instrumental in managing quality systems and documentation processes. Her role involves ensuring compliance with regulatory standards and enhancing quality assurance protocols. Trier's leadership in change control processes has been significant in maintaining the integrity of Kite Pharma's quality management systems, contributing to the company's reputation in the biotechnology industry.
Education and Expertise
Lorey Trier studied at the University of Phoenix, where she gained foundational knowledge that supports her expertise in quality management within the biotechnology sector. She possesses extensive experience in implementing GxP standards and ISO 13485 compliance, which are critical in ensuring product quality and safety. Trier's educational background and professional experience have equipped her with the skills necessary to excel in quality assurance and documentation processes.
Background in Quality Management
Prior to her current roles, Lorey Trier worked at Baxalta as a Sr. Quality Manager from 1996 to 2016, accumulating 20 years of experience in quality management. During her tenure at Baxalta, she developed a proven track record of enhancing quality system documentation processes. Her extensive background in managing quality systems has provided her with a deep understanding of compliance and documentation requirements in the biotechnology industry.