Senior Manager, CNC Operations

4 weeks ago

Akron, Ohio, United States Bristol-Myers Squibb Full time
Job Summary

We are seeking a highly skilled Senior Manager, CNC Operations to join our team at Bristol-Myers Squibb. As a key member of our production team, you will be responsible for executing process, assuring adherence, and optimizing execution of personnel, flow, and waste movement for production areas supporting MSS and Value Stream operations within CAR T clinical and commercial operations in multiple cGMP cleanroom suites.

Key Responsibilities
  • Ensure execution of cGMP, cleanroom requirements, and flow application to enable timely, compliant, and efficient completion of production tasks for Cell Therapy products.
  • Take personal responsibility to work safely and drive accountability and process for team members to do the same.
  • Accountable for the Process Documentation produced by teams and effective documentation for business processes.
  • Understand Cell Therapy production steps and sequence for each Unit Operation, role model good execution and behaviors for team members.
  • Actively define work priorities and adjust as necessary to align with site and or functional priorities.
  • Reports out performance metrics and goal progress daily, weekly, monthly in functional and site Tier meetings.
  • Drive completion, adherence to training requirements, and assess appropriate level of training for team members.
  • Monitors team training due dates and maintains the trained status of all team members.
  • Building a high performing team and help 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.
  • Conduct regular 1:1 meetings/skip levels with team members, leaders, and stakeholders 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.
  • Define strategic projects, change controls, and CAPAs as required to restore area performance and ensure optimal compliance levels.
  • Effectively control expenses within their influence (OT, Supplies, T&E).
Requirements
  • Bachelor's degree in supply chain, engineering, life sciences, information systems, business management, or related fields.
  • 5+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment.
  • 5+ years' experience in manufacturing and supply chain areas.
  • 3+ 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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