Manager, Label Operations

Role: Label Operations Manager at Bristol Myers Squibb's S12 Cell Therapy manufacturing site, responsible for overseeing clinical and commercial label management activities to ensure GMP compliance, patient safety, and regulatory adherence. Responsibilities include leading and motivating the Label Operations team, managing label control processes, supporting system implementation projects, and maintaining SOPs and quality metrics. The role involves coordinating with cross-functional teams for launch readiness and process improvements, as well as developing staff and ensuring continuous compliance with industry standards and regulations. Requirements: Bachelor’s degree or equivalent, at least 5 years of experience in cGMP-regulated pharma, biologics, or cell therapy manufacturing, and minimum 2 years of leadership experience. Skills in GMP, quality systems, risk management, and team development are essential. High-Value: biologics/cell therapy, GMP compliance, GMP label control, clinical and commercial labels, system implementation, cGMP and global regulatory standards, and leadership in a manufacturing environment. Work setup: Night shift, onsite in Summit, NJ; role involves collaboration with Quality, Manufacturing, and Regulatory teams.