CAR-T Cell Therapy Manufacturing Associate - Day Shift

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 39,000 - 47,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off

Holiday benefits

Job summary

Bristol Myers Squibb is hiring a Manufacturing Associate for the CAR-T team in Summit, NJ. You will manufacture human blood-derived components inside a cGMP cleanroom, following batch records and SOPs under supervision.

Responsibilities include operating within controlled processes, ensuring safety, completing documentation, and supporting quality investigations. Onsite day shift with a strong emphasis on compliance and teamwork.

Qualifications

• Knowledge of cGMP/FDA regulated industry.
• Basic mathematical skills.
• General understanding of cGMPs.
• Technical writing capability.
• Proficient in MS Office applications.
• Inventory control and/or management.
• Understanding of biology/chemistry/clinical practices.

Responsibilities

• Create inclusive culture that builds relationships with support groups.
• Execute operations per SOPs, batch records, and forms.
• Perform transactions in electronic systems and follow continuity processes.
• Prioritize safety of self and others.
• Report safety events within 24 hours.
• Escalate issues impacting compliance or safety.
• Complete documentation per governing documents.
• Work in a cleanroom environment applying aseptic processing.
• Maintain environmental conditions per regulatory specs.
• Refine manufacturing processes to improve efficiency.

Skills

GMP knowledge

Mathematical skills

Technical writing

MS Office proficiency

Biology/chemistry knowledge

Inventory management

cGMP familiarity

Education

High school diploma or equivalent; associate/bachelor preferred

Job description

Bristol Myers Squibb is hiring a Manufacturing Associate for the CAR-T team in Summit, NJ. You will manufacture human blood-derived components inside a cGMP cleanroom, following batch records and SOPs under supervision.

Responsibilities include operating within controlled processes, ensuring safety, completing documentation, and supporting quality investigations. Onsite day shift with a strong emphasis on compliance and teamwork.