Leah Hockenberry

Leah Hockenberry has a diverse work experience in the field of quality assurance and management. Leah began their career as a Technical Writer, Quality Engineering contractor at 3M - Detroit Abrasives in 2003. Leah then joined King Pharmaceuticals as a Quality Control Analyst from 2003 to 2005.

Leah gained experience as a Quality Assurance/Quality Control Specialist at Genesis Pharmaceuticals - Pierre Fabre from 2005 to 2006. Leah then worked as a Quality Assurance Specialist at VGXI, Inc., where they implemented quality systems and ensured compliance with cGMP and cGLP regulations.

In 2007, Leah became a Quality Assurance Associate at Introgen Therapeutics, Inc. Leah later joined Lexicon Pharmaceuticals as a Quality Systems Specialist, overseeing GMP and GCP quality systems, and as a Manager of Quality Assurance, responsible for GxP compliance and quality oversight of contract manufacturers.

Leah worked at Pall Corporation as a Quality Assurance Manager in 2015 before joining Bryllan, LLC. At Bryllan, they took on the role of Quality Systems Manager, managing the Quality department and ensuring company-wide compliance. Leah also served as a Process Engineer, developing and validating pharmaceutical manufacturing processes.

In 2017, Leah established their own consultancy firm, L. Hockenberry Consulting, where they served as President and CEO. Leah provided consulting services in quality assurance and management.

Currently, Leah is working as a Senior Manager, QA Operations at Sage Therapeutics.

Leah Hockenberry obtained their Bachelor of Science (BS) degree in Chemistry from Alma College, where they studied from 1998 to 2002.