Manufacturing Associate, CAR-T, Manufacturing Operations

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.

About the role

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.

Responsibilities

• Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
• Support deviation investigations and write-ups as needed.
• Support on-time closure of any assigned CAPAs within the designated shift.
• Aseptic technique and gowning is required for most activities: welding, connections, and transfers, at minimum.
• Aseptic ISO7/ISO5 qualification is required.
• Weighs 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, concise, format according to proper GDPs.
• Works in a team-based, cross-functional environment to complete production tasks required by shift schedule.
• Motivated, team-conscious individuals are needed to fulfill job requirements.
• Become a SME and qualified trainer within a designated function of manufacturing.
• Maintains 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.
• Ensures all documentation is correct and addresses procedural/documentation errors expeditiously and effectively.
• Records patient material handling data and information in a clear, concise, format according to proper GDPs.
• Able to problem-solve with minimal supervision.

Requirements

• High School Diploma required.
• Bachelor's or associate degree preferred.
• 0-1 years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.

Skills

• Knowledge of cGMP/FDA regulated industry.
• Basic mathematical skills.
• General understanding of cGMPs.
• Technical writing capability.
• Proficient in MS Office applications.
• Understanding of biology, chemistry, medical or clinical practices.

Benefits

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Pay

$27.83 - $33.72 per hour

Schedule

• Quad 2: Sunday - Wednesday (e/o Wednesday off), Onsite Night Shift, 5 p.m. - 5:30 a.m.
• Quad 4: Wednesday - Saturday (e/o Wednesday off), Onsite Night Shift, 5 p.m. - 5:30 a.m.