Tanya Lazur

Associate Director, Quality Assurance @ Travere Therapeutics

About Tanya Lazur

Tanya Lazur serves as the Associate Director of Quality Assurance at Travere Therapeutics in San Diego, California, where she has worked since 2020. With a background in quality assurance spanning over two decades, she has held various positions in notable companies, demonstrating expertise in Veeva Quality Vault Systems and auditing standards.

Work at Travere Therapeutics

Tanya Lazur has been serving as the Associate Director of Quality Assurance at Travere Therapeutics since 2020. In this role, she oversees quality assurance processes and ensures compliance with industry standards. Her tenure at Travere spans four years, during which she has contributed to the company's quality management systems and regulatory compliance efforts. Prior to her current position, she also held the role of Senior Manager of Quality Assurance at Travere from 2017 to 2020.

Education and Expertise

Tanya Lazur holds a Bachelor of Science degree in Biology from Northeastern University. She possesses extensive expertise in managing Veeva Quality Vault Systems, particularly in areas such as QualityDocs, Quality Management Systems (QMS), and Learning Management Systems (LMS). Her educational background and professional experience equip her with the knowledge necessary to navigate complex quality assurance challenges in the biotechnology sector.

Background in Quality Assurance

Tanya Lazur has a robust background in quality assurance, having worked in various roles across multiple organizations. She began her career at Pfizer as a Team Leader in QA Product Support from 2001 to 2003. Following this, she worked at Thermo Fisher Scientific as a Senior QA Specialist from 2011 to 2015. She then served as Quality Assurance Manager at HUYA Bioscience International from 2015 to 2017, and as a Senior QA Specialist at Vical for 11 months in 2017.

Auditing Skills and Standards

Tanya Lazur possesses auditing skills in several regulatory standards, including Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO 9001, Research Use Only (RUO), and Investigational Use Only (IUO). Her proficiency in these standards supports her role in ensuring that quality assurance practices meet regulatory requirements and industry expectations.

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