Job Description
Position Summary :
The Quality Manager (GMP) will be responsible for performing and managing day-to-day activities surrounding manufacture, testing and disposition for clinical study material. This will play a key role in overseeing all quality-related aspects of our outsourced manufacturing processes. This position is responsible for ensuring that products meet internal quality standards and comply with applicable regulatory requirements (e.g., FDA, EMA, GMP). As a liaison between the company and our contract manufacturing organization (CMO), the QA Manager will manage quality systems, review and approve batch records, handle deviations, and ensure proper documentation practices.
Key Responsibilities :
Qualifications :
About Upstream Bio :
Upstream Bio is a public company based in Waltham, MA.
We are a clinical-stage biotechnology company developing treatments for inflammatory diseases, with an initial focus on severe respiratory disorders. We are developing verekitug, the only known antagonist currently in clinical development that targets the receptor for thymic stromal lymphopoietin (TSLP), a cytokine which is a clinically validated driver of inflammatory response positioned upstream of multiple signaling cascades that affect a variety of immune mediated diseases. Upstream Bio has advanced this highly potent monoclonal antibody into separate Phase 2 trials for the treatment of chronic rhinosinusitis with nasal polyps (CRSwNP), severe asthma and chronic obstructive pulmonary disease (COPD). Our team is committed to maximizing verekitug’s unique attributes to address the substantial unmet needs for patients underserved by today’s standard of care. To learn more, please visit www.upstreambio.com.
Quality Manager • Waltham, MA, US