Cell Therapy Manufacturing Supervisor Liso-Cel PM Shift

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Supervisor, CAR T Manufacturing, Liso-cel

Position Overview

Oversee and lead a team of associates in the manufacture of human blood derived components per Batch Records and Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment. Shift Supervisors adhere 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.

This organization operates 24 hours a day, 7 days a week, 365 days a year. Selected candidates will be required to work one of the following shifts:

Quad 2: Sunday – Tuesday & every other Saturday, 5pm – 5:30am

Quad 4: Wednesday – Friday & every other Saturday, 5pm – 5:30am

These shifts receive a 15% shift differential in addition to regular salary

Duties and Responsibilities

Performance manage, train and oversee a team of associates in the production of blood component lots through any of the following areas: selection, activation, cell culture, harvest, and cryopreservation.

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.

Ensure all associates on the shift complete training assignments to ensure the necessary technical skills and knowledge. 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.

Write manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements

Work with production planning and area Management to establish daily unit operations schedule 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.

Ensure the shift works effectively in a team based, cross-functional environment to complete all production tasks required by shift schedule.

Collaborates closely with other Shift Supervisors to ensure seamless pass down and communication of operational status.

Other duties may be assigned, as necessary.

Required Competencies:

Knowledge/ Skills, and Abilities:

Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique

Knowledge of cGMP/FDA regulated industry

Basic mathematical skills

General understanding of cGMPs

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.

Required Education and Experience

Bachelors in a biologic science or engineering discipline, or relevant work experience including 3-6 years of experience in cGMP biologics cell culture manufacturing.

Experience in cell therapy manufacturing, or knowledge of the JCAR017 process is highly preferred.

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.

Cryopreservation processes and equipment.

Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.

Must have the ability to work assigned shift (Day, Night, Weekends and/or Holidays).

.

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 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 in close proximity to strong magnets

Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum.

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 the resources to pursue their goals, both at work and in their personal lives.

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, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com