Values: Leads by example and drives their team to adhere to the BMS values of Inclusion, Accountability, Innovation, Urgency and Passion. GMP: Is accountable to ensure their Manufacturing Managers and their WCT members execute the manufacturing of Cell Therapy products according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs). Responsible to own, review, author, or approve SOP, WI, master batch records. Safety: Takes personal responsibility to work safely and to ensure their managers and WCT members do the same. Performs regular safety Gemba walks, knows the hazards associated with their work and demonstrates safe behavior. Operates and maintains equipment to prevent injuries or incidents. Documentation: Is accountable for the Production Records produced by their Manufacturing Managers and WCT members. Performs batch record reviews (BRR) or Electronic Batch Record review by exception. Ensures that all documentation produced by their Managers and WCTs follows the ALCOA+ principles. Ensures the documentation produced by their Manufacturing Managers and WCT members is right first time, and all records and logbooks are complete and accurate. Resolve documentation errors and corrections as needed to enforce manufacturing turnaround-times. Ensures that their Manufacturing Managers and their WCTs have the appropriate level of training necessary for CAR-T GMP manufacturing in a multi-product commercial facility. Ensures that their Manufacturing Managers and their WCT members are proficient and qualified to perform the manufacturing tasks before doing so. Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Is required to perform Cell Therapy manufacturing to maintain hands on expert knowledge of each Unit Operation, demonstrate what good execution looks like to new managers and WCT members and when necessary, back fills for absent team members or makes up the execution resource requirements to meet the production schedule. Supports Material Review Board (MRB) data collection and provides process expertise when required to support the MRB decision making process. Rotates weekend coverage for manufacturing operations and is first line support for any technical or manufacturing issues during weekend coverage. Continues to develop expertise in the field of CAR - T Manufacturing and regulatory requirements that pertain CAR T manufacturing. Resource Management: Is responsible to provide the Production Scheduling team with information (daily, weekly monthly) on the availability of their managers and WCT production resources and tracks/maintains records of all team members actual availability vs planned or unplanned absence due to holidays, sickness, or other reasons. Is responsible to hire personnel that meet job description criteria and BMS values and sustain the manufacturing culture and that meet budgetary and fiscal requirement. Priorities: Sets their managers and WCTs priorities and adjusts as necessary to track the site and or functional priorities, establishes the WCT goals and is responsible to monitor, measure and assess the performance/completion of the WCT manufacturing activities and goals. Reports out performance metrics and goal progress daily, weekly, monthly in functional and site Tier meetings and the site metric control plans. Extensive knowledge of EHS and cGMPs and the know-how to work and manage within a regulated environment. Demonstrates aptitude for biotechnology principles and manufacturing systems. Demonstrated proficiency in selection of team and effectively managing personnel issues. Adaptable to a fast paced, complex, and ever-changing business environment. Knowledge of lean manufacturing principles required. Green belt certified is a preference. Excellent communication skills (EN). Bachelor's degree in related field is preferred, or equivalent in work experience, and the ability to think and lead strategically. Advanced degree preferred. 7+ years of relevant manufacturing experience in bulk biologic or cell therapy manufacturing. Minimum of 5 years leadership experiences including the management of direct reports required with previous experience in team development. 2-3 years working with team on KPI's. 2-3 years with regulatory audit direct interactions or SME experience. Project Management experience. Previous experience working on a second shift highly desired. Quality experience. Ability to lift 25 pounds.