Senior Manager, Cryo Operations, Inventory Management Located In Summit, NJ

Bristol-Myers Squibb - Summit, NJ

Full-time - Mid Level

Summit, NJ

Chemical Manufacturing

About the position

The Senior Manager, Cryo Operations & Inventory Management at Bristol Myers Squibb is responsible for overseeing the processes related to inventory, disposal, and planning for the storage of cryogenically frozen sample vials and patient materials within CAR T clinical and commercial operations. This role ensures compliance with regulatory standards and efficient operations in a cGMP multi-cleanroom suite, playing a critical part in the CAR T production processes.

Responsibilities

• Ensure compliant and efficient completion of production tasks for Cell Therapy products according to cGMP's and approved SOPs.
• Take personal responsibility for safety and drive accountability among team members, performing regular safety Gemba walks.
• Accountable for process documentation for inventory management and execute LIMS, MRP or Electronic Batch Record reviews.
• Maintain expert knowledge of each Unit Operation and model good execution for team members.
• Provide Supply Chain teams and site leadership with information on storage resources and task execution.
• Adjust activities to align with site priorities and report performance metrics in meetings.
• Drive completion of training requirements for self and team members, ensuring proficiency in production tasks.
• Build a high-performing team by recruiting exceptional people and providing feedback to employees.
• Conduct regular meetings with team members to mentor and develop individuals.
• Lead troubleshooting activities and manage deviations, ensuring timely reporting and resolution.
• Build trust and collaboration with peers and stakeholders across the company.
• Define strategic projects and change controls to restore area performance and compliance levels.
• Control expenses within their influence and lead by example in adhering to BMS values.

Requirements

• Bachelor's degree in supply chain, engineering, life sciences, information systems, business management or related fields.
• 5+ years relevant work experience in a regulated pharmaceutical manufacturing environment.
• 5+ years' experience in manufacturing and supply chain areas.
• 3+ years direct supervisory experience.
• Understanding of cell culture, cryopreservation, purification, and aseptic processing.

Nice-to-haves

• Advanced knowledge of cGMP/GDP/Pharmaceutical regulations and applications.
• Strong knowledge of inventory management principles and best practices.
• Proficiency in ERP systems / LIMS Applications and analytics tools.
• Strong written and verbal communication skills.

Benefits

• Competitive salary and benefits package
• Opportunities for professional development
• Flexible work environment
• Health and wellness programs