Why This Role Stands Out
Step into a crucial role at Abzena, a leading CDMO dedicated to bringing vital medicines to patients, where you'll gain hands-on experience in GMP manufacturing and quality operations. You'll thrive here if you're detail-oriented and eager to collaborate with cross-functional teams to ensure the highest quality standards. This is an excellent opportunity to grow your career in pharmaceutical quality assurance.
Quick Overview
Job Description
The Associate I, Quality Operations provides day‑to‑day QA oversight and documentation review to support GMP manufacturing of intermediates and drug substances. The role ensures production activities are executed in compliance with cGMP requirements through on‑floor QA presence, batch record review, and support of batch disposition. The position works closely with Manufacturing, QC, and other Quality functions to identify, escalate, and resolve issues in real time.