Manufacturing Associate - Summit West, NJ

Military Spouse Corporate Career Network • Summit West, NJ

8d • Onsite

About The Position

Bristol Myers Squibb is seeking motivated individuals to join their Cell Therapy team as Manufacturing Associates. This role involves manufacturing human blood-derived components in a controlled, cGMP cleanroom environment, adhering to strict regulatory requirements and standard operating procedures. The position offers opportunities for growth and development within a challenging and meaningful work environment focused on transforming patient lives through cell therapy. The company emphasizes work-life balance and offers a variety of competitive benefits and programs. The Cell Therapy team is at the forefront of reimagining the future of cell therapy, aiming to unlock its full potential and help patients on the path to a cure.

Requirements

• High School Diploma required.
• 0-1 years of cGMP cell therapy manufacturing, or bioprocessing manufacturing.
• 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.
• Aseptic qualification is required.

Nice To Haves

• Bachelor's or associate degree preferred.

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.
• Perform aseptic technique for tube welding, connections, and transfers.
• Weigh and measure in-process materials to ensure proper quantities are added/removed.
• Adhere to the production schedule ensuring on-time, internal production logistics.
• Record production data and information in a clear, concise, format according to proper GDPs.
• Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
• Work in a team-based, cross-functional environment to complete production tasks required by shift schedule.
• Become a SME and qualified trainer within a designated function of manufacturing.
• Maintain on-time completion of training assignments to maintain necessary technical skills and process knowledge.
• Perform other tasks as assigned, such as continuous improvement projects, inspection readiness, and right-first-time initiatives.

Benefits

• Competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED