Associate Director/Director, GMP Quality Assurance Operations
Full-timeEntryOpeningsOncologyAntibodiesMasters
Description
Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies either as single agents or as part of combination regimens to treat a range of solid tumors. For more information, visitwww.crescentbiopharma.comand follow the Company onLinkedInandX.
We are seeking an Associate Director/Director, GMP Quality Assurance Operations to be a key leader within Crescent’s Quality organization, responsible for providing hands-on Quality Operations oversight for GMP manufacturing activities supporting one or more of Crescent’s bispecific antibody and/or antibody-drug conjugate (ADC) programs. You will oversees quality activities across the manufacture of master cell bank, working cell bank, drug substance, and drug product/finished goods within a highly outsourced development and manufacturing model, and partners closely with the Senior Director of Quality and cross-functional teams to ensure phase-appropriate GMP compliance, effective execution of quality systems, and continuous inspection readiness while supporting aggressive development timelines.
Crescent Biopharma
PHARMACEUTICAL
Oncology Therapies
LocationWALTHAM, MA
Open Jobs11
Oncology
View Company ProfilePipeline
Self Help PlusN/A
A Novel Method of Screening for Ovarian Cancer Using Gynecologic Fluids and MucusN/A
Motivational interviewN/A
InfectedN/A
Folic acidN/A