Associate Director, Cryo Operations

2 days ago

Summit, New Jersey, United States Bristol-Myers Squibb Full time
Transforming Patients' Lives through Science

Bristol-Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking an experienced Associate Director, Cryo Operations to join our team in Summit, NJ.

About the Role

The Associate Director, Cryo Operations will lead a team of Senior Managers, Managers, Team Leads, and Associates responsible for all processes associated with the cryogenic storage infrastructure, planning, inventory management, and strategic outlook for the space within CAR T clinical and commercial operations.

Key Responsibilities
  • Ensure operation of equipment for cryogenic production tasks related to Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's)
  • Perform regular safety Gemba walks, identify hazards associated with team's work, and demonstrate safe behavior when operating and maintaining equipment
  • Accountable for inventory management records produced and needed by the team for procedural compliance
  • Working knowledge of Cell Therapy cryogenic production steps to maintain hands-on expert knowledge of each Unit Operation
  • Responsible for providing the Production Scheduling team with information on the availability, viability, and capability of equipment resources needed for task execution/progression
  • Actively set team priorities and adjust as necessary to align with site and or functional priorities
  • Drive completion, adherence to training requirements, and assess appropriate level of training for team members
  • Support building of a high-performing team of Operators and Supervisors, helps recruit exceptional people, conducts interviews/reviews candidate suitability, and provides meaningful feedback to current and future employees/leadership
  • Responsible for creating/managing Workday profiles for all new hired staff and administering the performance review process
  • Conducts regular 1:1 meetings with team members to mentor, develop/motivate individuals, and enable team members with their professional development
  • Lead troubleshooting activities for the team and provide ownership of Deviations occurring in area
  • Build trust and productive relationships with peers and stakeholders while driving collaboration across the company and external partners
Requirements
  • Bachelor's degree in supply chain, engineering, life sciences, information systems, business management, or related fields
  • 7+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment
  • 7+ years' experience in manufacturing and supply chain areas
  • 5+ years direct supervisor/personal management experience
  • Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
Working Conditions

Intermittent walking and sitting to perform job functions; however, ability to sit or stand for extended periods of time may be necessary

Physical dexterity to effectively use computers and documentation

Vision and hearing capability to work in job environment

Lift maximum of 25 pounds

Ability to work around laboratories and controlled, enclosed, restricted areas

Wear required cleanroom garments and personal protective equipment in designated areas

Makeup, gum, nail polish, or other potential microbial sources are prohibited in restricted areas

Exposure to reagents, chemicals, exposure to sanitization agents are expected, and potential exposure to human blood components

Areas may prohibit food, any outside materials, cell phones, and tablets

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