Manufacturing Associate

Bristol Myers Squibb EU Policy · West Summit, MA · Yesterday

On-siteResearch$27.83–$33.72/hrPart-time

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. Take your career farther than you thought possible.

About the role

Manufacturing Associates, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Responsibilities include:

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 is required for tube most activities: welding, connections, and transfers, at minimum.
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.
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.

Responsibilities

Support 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 is required for tube most activities: welding, connections, and transfers, at minimum.
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.
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.

Requirements

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

Qualifications

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.
Understanding of biology, chemistry, medical or clinical practices.

Skills

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.
Understanding of biology, chemistry, medical or clinical practices.

Benefits

At Bristol Myers Squibb, we recognize 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.

Pay

Summit West - NJ - US: $27.83 - $33.72 per hour

Schedule

Quad 1: Sunday - Wednesday (with every other Wednesday off), Onsite Day Shift, 5 a.m. - 5:30 p.m.
Quad 2: Sunday - Wednesday (with every other Wednesday off), Onsite Night Shift, 5 p.m. - 5:30 a.m.
Quad 3: Wednesday - Saturday (with every other Wednesday off), Onsite Day Shift, 5 a.m. - 5:30 p.m.
Quad 4: Wednesday - Saturday (with every other Wednesday off), Onsite Night Shift, 5 p.m. - 5:30 a.m.