Why This Role Stands Out
This role offers a fantastic opportunity to contribute to life-saving medicines, developing your skills in cutting-edge bioconjugation processes within a reputable CDMO. If you thrive in a collaborative, quality-focused environment and are eager to advance your career in biopharmaceutical manufacturing, this position is perfect for you to apply and make a real impact.
Quick Overview
Seniority
Mid Senior
Employment type
Full Time
Work mode
On Site
Location
Bristol, United States
Posted
9 hours 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/II is responsible for performing large-scale bioconjugation processes for cGMP manufacturing projects. The associate performs functions related to the manufacturing, development, and processing of drug substances, ensuring product compliance and multiple tasks that ultimately provide Good Manufacturing Practices and on time delivery to the customer. The individual must be able to communicate production status, communicate problems to proper personnel and understand how it affects other aspects of the operation.
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