CAR-T Manufacturing Team Lead Liso-cel (Night Shift)

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 53,000 - 64,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid holidays

Comprehensive benefits

Job summary

Bristol Myers Squibb in Summit, NJ is seeking a Manufacturing Team Lead for Liso-cel CAR-T Manufacturing Operations. You will oversee setup and operation of equipment, lead deviation investigations, and ensure on-time closure of CAPAs within the shift.

The role requires a senior associate level with cell therapy manufacturing experience; minimum degrees listed; strong GMP knowledge; you will train associates and act as supervisor when needed.

Qualifications

• Must be a Senior Associate in Cell Therapy Manufacturing.
• Bachelor’s degree with 2–4 years in cell therapy/biopharmaceutical operations.
• Associate / Medical Technical degree with 6+ years in manufacturing operations or a high school diploma with 8+ years experience.

Responsibilities

• Oversee equipment setup and operation to support production of blood component lots through cell culture, harvest, and cryopreservation.
• Lead deviation investigations and write-ups as needed.
• Accountable for on-time closure of CAPAs within the assigned shift.
• Adhere to aseptic technique and qualification requirements.
• Weigh and measure in-process materials to ensure correct quantities are added/removed.
• Maintain production schedule and internal logistics.
• Record production data clearly per GDP requirements.
• Perform tasks in line with site safety, quality systems, and GMP.

Skills

Cell culture

cGMP knowledge

Documentation

MS Office

Biology background

Team leadership

Problem solving

Education

Bachelor’s degree in biotech/biopharma

Assoc./Medical Tech degree

High School diploma/GED + 8+ years experience

Job description

Bristol Myers Squibb in Summit, NJ is seeking a Manufacturing Team Lead for Liso-cel CAR-T Manufacturing Operations. You will oversee setup and operation of equipment, lead deviation investigations, and ensure on-time closure of CAPAs within the shift.

The role requires a senior associate level with cell therapy manufacturing experience; minimum degrees listed; strong GMP knowledge; you will train associates and act as supervisor when needed.