Single Use Facility, Manufacturing Manager

Role: Manufacturing Manager leading shift operations in a biopharmaceutical production environment, focusing on therapeutic protein manufacturing under cGMP standards. Responsibilities: oversee execution of manufacturing unit operations—including bioreactors, chromatography, and automation systems—ensure compliance with SOPs and quality standards, manage team performance through training and development, maintain schedule adherence, and support process troubleshooting and continuous improvement. Qualifications: B.S. in science, engineering, biochemistry, or a related field; 6+ years biologic manufacturing experience, with supervisory or leadership expertise; strong knowledge of cGMPs, SOPs, and biopharma manufacturing processes. High-Value: biologics, therapeutic proteins, commercial manufacturing, cGMP compliance, leadership in a fast-paced, regulated environment. Work Setup: on-site at Devens, MA; no specific travel requirements stated.