Specialist, Lead Manufacturing Associate, Cell Therapy in Devens, MA

Bristol Myers Squibb; Harvard (MA); On-site; USD 60,000 - 100,000; Full time

Job summary

An innovative company is seeking a Specialist, Lead Manufacturing Associate to support cell therapy manufacturing operations. This critical role involves executing manufacturing processes, ensuring compliance with GMP regulations, and collaborating with cross-functional teams to drive technical solutions. With a focus on quality and safety, the position offers the chance to lead and train team members in a dynamic environment. Emphasizing work-life balance and diversity, this opportunity allows you to contribute to transformative projects that enhance patient outcomes in the rapidly evolving field of cell therapy.

Benefits

Competitive benefits

Work-life balance

Diversity and inclusion initiatives

Qualifications

• 4+ years of experience in cGMP cell therapy manufacturing or related fields.
• Knowledge of GMP regulations and manufacturing systems.

Responsibilities

• Execute manufacturing operations according to SOPs and batch records.
• Collaborate with teams to resolve technical issues and ensure compliance.

Skills

cGMP manufacturing

cell therapy processes

technical problem-solving

documentation compliance

Education

Associate or Bachelor's Degree

High School Diploma

Job description

Specialist, Lead Manufacturing Associate, Cell Therapy in Devens, MA

Join Bristol Myers Squibb as a Specialist, Lead Manufacturing Associate, Cell Therapy in Devens, MA.

This role involves supporting routine manufacturing operations for cell therapy programs, requiring knowledge of GMPs and a goal-oriented, flexible attitude. The position is critical for driving innovative cell therapy projects that transform patient lives.

Responsibilities include:

• Executing manufacturing operations according to SOPs and batch records
• Supporting documentation and compliance with GMP regulations
• Collaborating with cross-functional teams to resolve technical issues
• Leading and training team members to ensure quality and safety standards
• Participating in investigations, deviations, and CAPA processes
• Maintaining environmental and safety standards in a cleanroom environment

Qualifications:

• Associate or bachelor's degree preferred; high school diploma or equivalent required
• 4+ years of experience in cGMP cell therapy manufacturing or related fields
• Knowledge of cell therapy processes, GMP regulations, and manufacturing systems

Shift:

Available shift: 2, 6pm - 6am, rotating including holidays and weekends.

Additional Information:

We offer a supportive environment with competitive benefits, emphasizing work-life balance, diversity, and innovation. Bristol Myers Squibb is committed to reimagining cell therapy and improving patient outcomes. We encourage applications from diverse candidates and provide accommodations during the recruitment process.