Cell Therapy Manufacturing Manager

Bristol Myers Squibb EU Policy; Bothell (WA); On-site; USD 114,000 - 138,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Medical/dental/vision insurance

Job summary

Bristol Myers Squibb in Bothell, WA is seeking a Manufacturing Manager I to lead and drive the execution of cGMP cell therapy manufacturing processes, mentoring a team and guiding cross-functional collaboration to ensure safety, compliance, and reliable production.

You will manage SOPs, batch records, change controls, MRB activities, training, and continuous improvement, while maintaining inspection readiness and working in a highly regulated environment.

Qualifications

• 5+ years in cGMP cell therapy manufacturing or related field with 2 years of leadership experience (lead or equivalent).
• Experience in cell therapy manufacturing and aseptic processing.
• Proven performance management responsibilities.
• Knowledge of Change Controls and MRB processes.
• Ability to write and review GMP documentation and training materials.

Responsibilities

• Manage creation and compliance of Source Governing Documents related to cell therapy operations.
• Oversee operations within validated manufacturing systems.
• Plan, resource, and oversee daily activities while controlling costs.
• Maintain clean, compliant, inspection-ready facilities and equipment.
• Drive right-first-time initiatives and address compliance issues.
• Lead change controls, deviations, and investigations to closure.
• Develop corrective/preventive actions and CAPA programs.
• Ensure training and GMP compliance for all staff.
• Hire, mentor and develop personnel and conduct performance reviews.

Skills

Leadership

Troubleshooting

Performance management

Teamwork

Data analysis

Education

Bachelors in science or engineering

Job description

Bristol Myers Squibb in Bothell, WA is seeking a Manufacturing Manager I to lead and drive the execution of cGMP cell therapy manufacturing processes, mentoring a team and guiding cross-functional collaboration to ensure safety, compliance, and reliable production.

You will manage SOPs, batch records, change controls, MRB activities, training, and continuous improvement, while maintaining inspection readiness and working in a highly regulated environment.