Quality Assurance Associate I — GMP/GLP Documentation

A leading biotechnology firm in San Diego is looking for a self-motivated team member to support clinical product launches. The role involves batch record reviews, managing controlled documentation, and coordinating investigations related to production deviations. Candidates should have a Bachelor’s Degree and have at least 2 years of experience in a cGMP environment, along with strong communication and detail-oriented skills. The position offers a salary range of $65,000 - $75,000 annually, along with a comprehensive benefits package. #J-18808-Ljbffr