**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . At **Bristol Myers Squibb** , we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. **Position Summary:** Serve as a lead associate in the manufacture of human blood derived components per Batch Records and Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment. Lead Manufacturing Associate adheres to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Support the quad manager for communication of production deviations, review of executed batch records and assistance with quality investigations are required, as applicable. The Lead Manufacturing Associate works closely with the Quad Manager and serves to supervise the shift when the manager is not available. The Lead Manufacturing Associate is also a qualified trainer for all buckets of operation. **Shifts Available:** Breyanzi Selection - Third Shift, 9:30pm - 5:30am **Required Competencies:** + Thorough understanding of media production (if applicable), cell culture, selection/isolation, activation/initiation, transduction, debead (if applicable), expansion, harvest and cryopreservation for CAR-T + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. + Basic mathematical skills + Full compliance with Good Documentation Practices + Technical writing capability + Proficient in MS Office applications + Proficient in BMS Business Applications including Syncade/MES/Oracle, EQRMS/Infinity, Cellabs + Background to include an understanding of biology, chemistry, medical or clinical practices + Experience in any of the following areas is required: (Aseptic processing in ISO 5 biosafety cabinets, Universal precautions for handling human derived materials in BSL-2 containment areas, Cell expansion using incubators and single use bioreactors, Cell washing processes and automated equipment, Cell separation techniques and automated equipment, OR Cryopreservation processes and equipment) + Must have the ability to work assigned shift (Day, Night, Weekends and/or Holidays) + Experience as a trainer for GMP manufacturing processes **Key Responsibilities:** + Production of blood component lots for one CAR-T bucket of operations + Cross trained in all other buckets of operations (based on availability and business need) + Provide training and guidance to manufacturing associates as required. + Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum. + Aseptic qualification required per bucket + Weigh and measure in-process materials to ensure proper quantities are added/removed. + Perform and oversee process unit operations described in standard operating procedures and batch records. + Complete and review documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. + Assist Manager to ensure the shift performs tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. + Serve as a qualified trainer to maintain the shift at an acceptable qualification standard. + Support deviation investigations and on-time closure of deviations and CAPAs. + Work with Manager to schedule daily unit operations that includes people, product, and material flow across multiple shifts. + Ensure associates execute scheduled activities on-time, in accordance with the production schedule. + Ensure the batch records for production data and all information are in a clear, concise, format according to proper GDPs. + Help to ensure the shift works effectively in a team based, cross-functional environment to complete all production tasks required by shift schedule. + Collaborates closely with Managers to ensure seamless pass down and communication of operational status. + Other duties may be assigned, as necessary. + No direct reports will be assigned to this job role. **Qualifications & Experience:** + Bachelor's degree and 2-4 years of experience in cell therapy of + Biopharmaceutical operations. + Associate / Medical Technical degree and 6+ years of Manufacturing + Operations experience + High School diploma/GED and 8+ years of Manufacturing or Operations experience. **Working Conditions:** + Intermittent walking, standing and sitting to perform job functions; however, ability to stand for extended periods of time may be necessary. + Must be comfortable working with contained human blood components. + Physical dexterity sufficient to use computers and documentation. + Sufficient vision and hearing capability to work in job environment. + Ability to lift 25 pounds. + Must have the ability to work in laboratories and controlled, enclosed, restricted areas. + Must be able to be near strong magnets + Must be comfortable being exposed to human blood components. + Cleanroom garments and personal protective equipment will be required in designated areas which cover head, parts of the face, core body, and legs/feet. + Makeup, gum, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas. + Flexibility to don clean room garments and personal protective equipment (PPE). + Clean room environment is an enclosed, restricted space, with assigned pressure and temperature conditions. + Reagents, chemicals, and exposure to sanitization agents are expected. + Routine exposure to human blood components. + Restricted areas prohibit food, any outside materials such as cell phones, tablets, at a minimum. + Work from home is not approved for this role **Why You Should Apply:** Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMSCART VETERAN \#LI-Onsite \#NIGHT_SHIFT_OPS If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1586490 **Updated:** 2024-11-10 02:20:21.003 UTC **Location:** Summit West-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.