Senior Cell Therapy Manufacturing Associate Night Shift

Bristol-Myers Squibb Company; Harvard (MA); On-site; USD 46,000 - 56,000; Full time

Benefits offered by this job

Flexible Time Off

11 paid company holidays

Comprehensive benefits

Job summary

Bristol Myers Squibb Company is seeking a Senior Manufacturing Associate, Cell Therapy, to support routine manufacturing operations in a compliant, safe, and efficient manner at our Devens, MA facility. The role requires working in a GMP environment, performing aseptic processing, and adapting to rotating shifts.

The candidate should have a strong background in cell therapy manufacturing, experience with automated equipment, and the ability to train others and participate in investigations.

Qualifications

• High school diploma and 3+ years of experience in cGMP bioprocessing or cell therapy manufacturing.
• Bachelor’s degree in a relevant science or engineering field is strongly preferred.
• Knowledge of cGMP regulations and FDA guidance for biologics and cell therapy manufacturing.
• Able to work in a cleanroom and perform aseptic processing.

Responsibilities

• Execute operations per SOPs and batch records.
• Maintain safety, quality systems and GMP compliance.
• Complete training and SOPs for operations.
• Assist in setting up manufacturing areas and equipment.
• Write manufacturing operating procedures and ensure efficiency.
• Work with production planning on daily unit operations schedules.
• Support investigations and identify innovative solutions.

Skills

cGMP knowledge

Aseptic processing

Cell therapy manufacturing

Automated equipment

Cell washing / cryopreservation

Cleanroom operations

Shift flexibility (Day/Night/Weekends)

Education

High school diploma + 3+ years cGMP experience

Bachelor's in science or engineering (preferred)

Tools

Automated equipment

Single-use bioreactors

ISO 5 biosafety cabinets

Job description

Bristol Myers Squibb Company is seeking a Senior Manufacturing Associate, Cell Therapy, to support routine manufacturing operations in a compliant, safe, and efficient manner at our Devens, MA facility. The role requires working in a GMP environment, performing aseptic processing, and adapting to rotating shifts.

The candidate should have a strong background in cell therapy manufacturing, experience with automated equipment, and the ability to train others and participate in investigations.