Manufacturing Associate, CAR-T Media Prep

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.

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.

Manufacture cell culture media preparation in support of S12 CAR T manufacturing per Standard Operating Procedures (SOPs) in a controlled, cleanroom environment.

Shifts Available:

• This position is for Quad 1 Sunday to Tuesday, with every other Wednesday, from 6:00 am to 6:30 pm

Responsibilities:

• Perform set-up and operation of equipment to support production of media and solution preparation to support cell culture processes.
• Aseptic technique is required for most activities: welding, connections, and transfers, at minimum. Aseptic qualification and gowning is required.
• Perform activities in biological safety cabinets.
• Support deviation investigations and write ups as needed.  Support on time closure of any assigned CAPAs within the designated shift.
• Weighs, calculates, and measures in-process materials to ensure proper quantities are added/removed.
• Adheres to the production schedule ensuring on-time, internal production logistics.
• Records production data and information in a clear and concise format according to proper GDPs, adhering to ALCOA+ principles.
• Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
• Works in a team based, cross-functional environment to complete production tasks required by shift schedule.
• Motivated, team consciousness individuals are needed to fulfill job requirements. 
• Become a SME and qualified trainer within a designated function of manufacturing.  Supervision will be managed by the shift Supervisor or designated Team Lead.
• Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.
• Performs other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc.

Knowledge & Skills:

• Understanding of media and buffer preparation requirements for cell culture, and aseptic processing or lab techniques.
• Familiarity with cGMP/FDA regulated industry.
• Basic mathematical skills.
• Ability to read, execute and document steps in a GMP batch record.
• Proficient in MS Office applications.
• Background to include a basic understanding of biology, chemistry, or pharmaceutical processing.

Pre-requisites:  Prior experience in Manufacturing and/or scientific/engineering education

Basic Requirements:

• Bachelor Degree
• OR Associate / Medical Technical degree and 2 years of Manufacturing or Operations experience
• OR HS Diploma / GED and 3 years of Manufacturing or Operations experience
   

Working Conditions:

• Intermittent walking and sitting to perform job functions; however, ability to sit or 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 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