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QA Associate I/II, Operations - Shift B

AbzenaBristol🇺🇸United StatesPosted Sep 9, 2026

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

Seniority

Mid Senior

Work mode

On Site

Location

Bristol, United States

Posted

5 weeks ago

Compliance

Job Description

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 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.