(Night Shift) Manager, Manufacturing, Cell Therapy

Bristol Myers Squibb; Harvard (MA); On-site; USD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a dedicated Night Shift Manager for their new Cell Therapy manufacturing facility. This pivotal role involves overseeing 24/7 operations, ensuring compliance with cGMP standards, and fostering a culture of teamwork and safety. The ideal candidate will have extensive experience in biologics manufacturing and a passion for leading teams in a dynamic environment. Join a company that values work-life balance and diversity, and contribute to groundbreaking advancements in cell therapy.

Benefits

Competitive benefits

Work-life balance

Diversity and inclusion initiatives

Qualifications

• 5+ years in cGMP biologics cell culture manufacturing.
• Bachelor's degree in a relevant science or engineering discipline.

Responsibilities

• Manage documentation and ensure compliance in manufacturing.
• Oversee daily operations and maintain safe working conditions.
• Lead investigations and implement training programs.

Skills

cGMP compliance

cell culture manufacturing

team leadership

documentation management

investigation and corrective actions

Education

Bachelor's degree in science or engineering

Job description

(Night Shift) Manager, Manufacturing, Cell Therapy

Join to apply for the (Night Shift) Manager, Manufacturing, Cell Therapy role at Bristol Myers Squibb.

This role supports the start-up and commercial licensure of a new Cell Therapy manufacturing facility in Devens, MA, overseeing 24/7 operations and managing manufacturing associates.

Responsibilities

1. Manage documentation, procedures, and policies to ensure compliance.
2. Oversee daily operations within validated manufacturing systems.
3. Maintain safe, efficient, and compliant operating areas.
4. Lead investigations, corrective actions, and preventative measures.
5. Implement and maintain training programs.
6. Foster a culture of teamwork, safety, and compliance.
7. Coordinate communication across departments regarding operational activities.
8. Supervise operators in GMP-compliant operations, documentation, and training.
9. Hire, mentor, and conduct performance reviews for staff.
10. Work in a clean room environment, with exposure to human blood components and magnetic fields.

Qualifications

• Bachelor's degree in a relevant science or engineering discipline or equivalent experience.
• At least 5 years of experience in cGMP biologics cell culture manufacturing.
• Preferred experience in cell therapy manufacturing, aseptic processing, and related techniques.

Additional Information

Shift: 6pm-6am, rotating weekends. This role requires working in a clean room environment and may involve holidays and weekends.

Bristol Myers Squibb values work-life balance and offers competitive benefits. We support diversity and inclusion and encourage applicants with diverse backgrounds to apply.