Lead Manufacturing Associate, Cell Therapy, Breyanzi - Harvest - Days (R1544336-en-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.Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS’s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.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. 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 Shift Supervisor and serves to supervise the shift when the supervisor is not available.This position is for one of the following shifts, Quad 1 (Sunday – Every other Wednesday 5:00 am - 5:30 pm), Quad 2 (Sunday – Every other Wednesday 5:00 pm - 5:30 am), Quad 3 (Every other Wednesday - Saturday 5:00 am - 5:30 pm) or Quad 4 (Every other Wednesday - Saturday 5:00 pm - 5:30 am). Start and end times are subject to change based on business demands.Duties and Responsibilities:
- Production of blood component lots through any of the following areas: selection, activation, cell culture, harvest, and cryopreservation. Provide training and guidance to manufacturing associates as required.
- Aseptic technique is required for most activities: tube welding, connections, and transfers, at minimum.
- 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.
- Ensure the shift performs tasks in a manner consistent with the safety policies, quality systems, and GMP requirements.
- Serve as a trainer to maintain the shift at an acceptable qualification standard.
- Lead deviation investigations and support on-time closure of deviations and CAPAs.
- Work with Shift Supervisor 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 Shift Supervisors to ensure seamless pass down and communication of operational status.
- Other duties may be assigned, as necessary.
- Bachelors in a biologic science or engineering discipline and 4+ years of experience, or relevant work experience
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
- Experience in any of the following areas is required: Aseptic processing in ISO 5 biosafety cabinets, CAR-T Selection, Cell expansion using incubators and single use bioreactors, Cell washing processes and automated equipment, CAR-T Harvest Operations
- Advanced understanding of cell culture and Selection, Activation through Expansion or Harvest Bucket operations
- Knowledge of cGMP/FDA regulated industry
- Basic mathematical skills
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.
- Technical writing capability
- Proficient in MS Office applications
- Background to include an understanding of biology, chemistry, medical or clinical practices
- Sufficient vision and hearing capability to work in job environment.
- 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).
- Intermittent walking and sitting to perform job functions; however, ability to sit or stand for extended periods of time may be necessary.
- Physical dexterity sufficient to use computers and documentation.
- Climb - Required to climb (use of stepladders in production areas, or stairwells) several times a day.
- Bend and Kneel - Required to bend or kneel several times a day.
- Overhead work - Required to perform overhead reaching during handling of production materials/files/supplies up to 25 pounds several times a day, throughout the day.
- Moving Head and Neck – Required movement of head/neck while using computer applications and handling of production equipment and materials several times a day, throughout the day.
- Twisting - Required movement of twisting waist while setting up equipment several times a day, throughout the day.
- Repetitive Use - Required repetitive use of arms/wrists/hands while setting up equipment and processing several times a day, throughout the day.
- Must have the ability to work around laboratories and controlled, enclosed, restricted areas.
- 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, or 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.
- Must be comfortable being exposed to human blood components.
- Must be able to be near strong magnets
- Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum.
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.
Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.
To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.
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 approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to email@example.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
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