Label Operations Lead, Cell Therapy

Bristol Myers Squibb; Summit (NJ); On-site; USD 104,000 - 125,000; Full time

Benefits offered by this job

11 paid company holidays

Flexible time off

Comprehensive benefits

Job summary

Bristol Myers Squibb is seeking a Label Operations Manager for the Summit West facility in Summit, NJ. You will supervise label control activities for CTDO, ensuring GMP-compliant label issuance and continuous improvement of processes.

You will lead a team, align with regulatory requirements, and drive timely labeling for clinical and commercial products. Strong GMP knowledge and leadership experience are essential for this role.

Qualifications

• Minimum 5 years of experience in pharmaceutical, biologics, cell therapy, or other cGMP-regulated manufacturing operations.
• Minimum 2 years of leadership experience with responsibility for team performance, development, and execution of manufacturing activities.
• Demonstrated experience operating in compliance with cGMP regulations, quality standards, and regulatory expectations.

Responsibilities

• Lead team to ensure Label Management and align with Global and Regional Regulatory requirements.
• Oversee daily activities of the Label Operations team at Summit, NJ.
• Issue clinical and commercial labels timely for in-process and final product labeling operations.
• Develop, manage, and onboard staff for label control.
• Write, review, and update SOPs; maintain GMP documentation and batch records.
• Develop quality metrics and monitor compliance.
• Collaborate with stakeholders to resolve quality system issues.

Skills

GMP knowledge

Quality risk management

Leadership

Regulatory understanding

Communication

Project coordination

Staff development

Decision making

Microsoft Office

Education

Bachelor's degree

Job description

Bristol Myers Squibb is seeking a Label Operations Manager for the Summit West facility in Summit, NJ. You will supervise label control activities for CTDO, ensuring GMP-compliant label issuance and continuous improvement of processes.

You will lead a team, align with regulatory requirements, and drive timely labeling for clinical and commercial products. Strong GMP knowledge and leadership experience are essential for this role.