Accountable to ensure completion of EM Monitoring Sampling tasks for Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP's) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs). Take personal responsibility to work safely and drive accountability and process for team members to do the same. Perform regular safety Gemba walks, identify the hazards associated with team's work and demonstrate safe behavior when operating and maintaining equipment to prevent injuries or incidents. Lead and ensure EM sampling responsibilities are performed in accordance with the organization's policies, procedures, state, federal and local laws. Drive compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory requirements. Drive completion, adherence to training requirements and assess appropriate level of training for team members, completes their training plan on time and ensures proficiency and qualification to perform the production tasks. Monitors team training due dates and maintain the trained status of all team members by ensuring appropriate time is allocated to training activities. Lead will collaborate with Supply Chain Scheduling, Abecma, Breyanzi, Media Prep and Warehouse Ops Management to ensure timely and accurate EM sampling of GMP areas. Scheduling EM Sampling for routine EM every week for the team. Lead will serve as the liaison to the QC teams for testing of EM samples. Communicate effectively with Manufacturing Operations peers, cross-functional peers and management. Assist in troubleshooting and solving problems with various functional groups to drive efficiency and productivity. Lead EM Sampling Team to perform Environmental Monitoring on a routine and non-routine basis under Static and Dynamic conditions for all S12/S16 and S6A GMP manufacturing and associated warehouse areas. Responsible to be the Point of Contact and Communication with Facilities and other functional groups during planned or unplanned events like Air Reversals to be able to pull together the team to perform EM Sampling for Suite Release. Under the guidance of management, support special project work and continuous improvement initiatives for MO. Perform Environmental Monitoring Sampling steps to maintain hands-on expert knowledge of each Unit Operation, role model good execution and behaviors for team members and if necessary, able to backfill execution resources to meet the production schedule. Actively set team priorities and adjust as necessary to align with site and or functional priorities, establishes the team goals and monitor, measure and assess the performance/completion of the team production 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. Lead troubleshooting activities for the team and provide ownership of Deviations occurring in area and Support and/or lead investigations & CAPAs associated with EM excursions Build trust and productive relationships with peers and stakeholders while driving collaboration across the company and external partners. Lead by example, role model leadership behaviors and drives their team to adhere to the BMS values of Inclusion, Accountability, Innovation, Urgency and Passion. 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. Expertise in Environmental Monitoring in aseptic and non-aseptic processing areas. Ability to stand for extended periods of time. Cleanroom garments and personal protective equipment will be required in designated areas which cover head, face, core body, arms/hands, and legs/feet. Position requires the ability to wear aseptic gowning (ISO7/ISO8). Must have strong technical writing capability to support deviation investigations, change control evaluations, and closure of CAPAs. Ability to support on-boarding and training of new EM associates. Ability to become gown qualified and perform EM duties within the warehouse, media, and cell processing suites. Advanced knowledge of cGMP/GDP/Pharmaceutical regulations and applications. Strong knowledge and application of OSHA, DEA, USP and other applicable WH regulations. Proficiency in systems like CELabs, CMMS and application use for business operations. Proficiency in MS Office applications. Proficiency in analytical, problem-solving, critical thinking skills and strong situational decision making. Proficient organizational and time management skills and Strong written and verbal communication skills. Ability to adapt to changing business conditions while maintaining appropriate level of controls and compliance with regulatory requirements. Flexible with the ability to adapt, respond quickly and manage change in a fast-paced environment. Ability to work independently, within prescribed guidelines, or as a team member. Demonstrates ability to follow detailed directions in a manufacturing cGMP environment. Reliable with ability to respond to challenges in a positive, and objective manner. Adaptable to dynamic conditions, work practices, and schedules. Able to communicate effectively with cross-functional areas and external agencies. Requires a High School diploma or equivalent. Associate or bachelor's degree in a scientific discipline preferred. 3 years demonstrated work experience in a cGMP environment. 1 year of leadership experience required. Strong MS Office skills. Strong understanding of GMP practices.