Cell Therapy Lab Technologist

About the role

Aseptic Processing | Cell Therapy | Biomanufacturing | Career Growth Join a cutting-edge biotechnology organization developing innovative cell-based therapies aimed at improving the lives of individuals with autoimmune diseases. This is an opportunity to work in a clinical-stage GMP manufacturing environment where you'll play a hands-on role in producing life-changing products while gaining exposure to advanced bioprocessing, quality systems, and cleanroom manufacturing.

Job Type: Contract to Hire. Location: Hudson, WI. Workplace: Fully onsite. Application Deadline: Oct 23, 2026.

Responsibilities

• Perform manufacturing and processing activities in a GMP cleanroom using aseptic and sterile techniques.
• Operate specialized laboratory and production equipment including cell processing, encapsulation, microscopy, and cell-counting systems.
• Prepare reagents, solutions, and materials to support manufacturing and laboratory operations.
• Accurately complete batch records, logbooks, and GMP documentation in accordance with Good Documentation Practices (GDP).
• Support quality initiatives, deviation investigations, environmental monitoring, and inspection readiness activities.
• Analyze production and laboratory data to support troubleshooting, process optimization, and continuous improvement efforts.
• Collaborate with Quality, Manufacturing, and R&D teams as the organization scales from development to commercial manufacturing.
• Maintain strict compliance with GMP regulations, SOPs, and biosecurity requirements.

Requirements

• Bachelor's degree in Biology, Chemistry, or a related science field (Associates degree with relevant industry experience also considered).
• 1+ year of experience in a GMP-regulated, pharmaceutical, biotech, or medical device environment.
• Hands-on laboratory experience with aseptic technique, sample handling, reagent preparation, and documentation.
• Experience working in cleanrooms or controlled manufacturing environments preferred.
• Strong attention to detail and the ability to follow SOPs while maintaining accurate records.
• Excellent communication and documentation skills.

Skills

• FDA-regulated manufacturing environments.
• Cell therapy, bioprocessing, biologics, or pharmaceutical manufacturing.
• Environmental monitoring, quality systems, and deviation investigations.
• Continuous improvement and process optimization initiatives.

Benefits

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan (Pre-tax and Roth post-tax contributions available)
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability