Quick Overview
Job Description
The Quality Control (QC) Associate I is responsible for performing analytical testing and laboratory activities that support stability, qualification/validation, and release testing of biologics in a cGMP-regulated environment. This role supports routine QC operations through the execution of analytical methods, data review, equipment maintenance, QC inventory management, and continuous improvement initiatives while ensuring compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and applicable regulatory requirements.
The successful candidate will demonstrate technical expertise, attention to detail, data integrity awareness, and a commitment to maintaining inspection readiness while supporting internal and client-driven programs.