Quick overview
SeniorityMid Senior
Employment typeFull Time
Work modeOn Site
LocationBristol, United States
Posted8 hours ago
Continuous Improvement
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 Supervisor, Quality Operations leads day-to-day QA oversight for GMP manufacturing of intermediates and drug substances. This role directs and develops Quality Operations personnel, while ensuring compliant execution of on-floor support, documentation review, environmental monitoring, and batch disposition activities.
The Supervisor plans and prioritizes team workload, provides technical guidance, escalates quality risks, and partners with Manufacturing, Analytical Services, and other Quality functions to resolve issues in real time. The position promotes inspection readiness, data integrity, operational excellence, and continuous improvement across site Quality Operations.
Shift A: 4 x 10, Sun-Weds
Shift B: 4 x 10, Weds-Sat