Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations

About the role

The Manufacturing Associate is responsible for producing human blood-derived components in a controlled, cGMP cleanroom environment in accordance with Standard Operating Procedures (SOPs) and regulatory requirements. This role operates within a collaborative, shift-based team structure and plays a critical part in ensuring the quality, safety, and timely delivery of life-changing therapies.

Responsibilities

• Set up and operate equipment to support blood component production through cell culture, harvest, and cryopreservation
• Apply aseptic technique for all applicable activities, including tube welding, connections, and transfers; aseptic qualification is required
• Weigh and measure in-process materials to ensure accurate quantities are added or removed
• Adequately adhere to the production schedule to support on-time, internal production logistics
• Record production data clearly and concisely in accordance with Good Documentation Practices (GDPs)
• Support deviation investigations and write-ups as needed
• Ensure on-time closure of assigned CAPAs within the designated shift
• Perform all tasks in alignment with site safety policies, quality systems, and GMP requirements

Requirements

• Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or laboratory technique
• Familiarity with cGMP and FDA-regulated industry standards
• Strong technical writing capability
• Basic mathematical skills with a general understanding of cGMPs
• Proficiency in Microsoft Office applications
• Background in biology, chemistry, or medical/clinical practices preferred
• Prior experience in manufacturing and/or a scientific or engineering discipline

Qualifications

• Bachelor's Degree—Associate's / Medical Technical Degree
• 3+ years in Manufacturing Operations
• High School Diploma / GED
• 2+ years in Manufacturing or Operations

Skills & Abilities

• Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or laboratory technique
• Familiarity with cGMP and FDA-regulated industry standards
• Strong technical writing capability
• Basic mathematical skills with a general understanding of cGMPs
• Proficiency in Microsoft Office applications

Benefits

Read more careers.bms.com/working-with-us.

Pay

$27.83 - $33.72 per hour

Schedule

Quad 1 — Sunday through Wednesday, 5:00 AM – 5:30 PM

Shift Schedule is subject to change based on business needs.