Sr QA Associate, Operations at Abzena Inc. – Bristol, Pennsylvania

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.

Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.

We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.

We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.

The Senior Associate, QA Operations is responsible for providing quality oversight of GMP manufacturing and development activities through direct quality presence on the manufacturing floor and review/approval of GMP documentation. This role ensures that manufacturing operations comply with cGMP regulations, internal procedures, and client requirements. The position serves as the primary QA partner to Manufacturing and Process Development teams, supporting batch execution, documentation review, deviation management, and real-time compliance oversight. The role requires strong knowledge of GMP requirements, attention to detail, and the ability to work cross-functionally in a fast-paced CDMO environment.

FLSA: Exempt