Supervisor, Manufacturing

Role: Supervisor of manufacturing operations at a commercial cell therapy facility, overseeing a team in a cGMP environment for cancer immunotherapies, specifically CAR T-cell products. Responsibilities: supervise daily manufacturing activities, develop and coach staff, generate SOPs and batch records, ensure compliance with regulations, monitor production schedules, investigate issues, and collaborate with vendors and cross-functional teams. Requirements: Master's degree with 3+ years or Bachelor's degree with 5+ years relevant manufacturing experience; strong knowledge of cGMPs, process troubleshooting, and electronic quality systems; leadership skills in team building and training. Preferred: cell culture experience, ability to work off-shift and on-call, excellent communication, adaptable mindset, and familiarity with FDA CFRs. High-Value: biologics manufacturing, cancer cell therapy, cGMP compliance, team leadership, and experience with process documentation and quality systems. Work Setup: night shift (Sun-Wed, 3:00 PM-1:30 AM), based in Frederick, MD, with potential for on-call duties.