Associate Specialist, Cell Therapy

Scorpion Therapeutics; California (MD); On-site; USD 82,000 - 123,000; Full time

Job summary

Scorpion Therapeutics is seeking a Manufacturing Technician to support cell therapy production in a GMP-regulated environment. You will execute manufacturing steps per batch records and SOPs, support equipment setup, monitor processing equipment, and maintain precise documentation to ensure compliant operations.

Responsibilities include deviation support, inventory control, and cross-functional collaboration with Manufacturing, Quality, and Process Development teams to maintain a compliant and

Qualifications

• 2+ years GMP or technical experience or an associate/bachelor's in science/engineering with 0-2 years experience.
• Understanding of cGMP, aseptic techniques, cleanroom procedures.
• Ability to follow detailed instructions and escalate issues appropriately.

Responsibilities

• Execute manufacturing steps per batch records, SOPs, and electronic instructions.
• Support equipment setup, material staging, and facility readiness.
• Monitor and operate processing equipment.
• Maintain documentation accuracy.
• Support deviation investigations, inventory control, and visual inspection activities.
• Collaborate across Manufacturing, Quality, Process Development, and other teams.

Skills

GMP knowledge

Aseptic techniques

Cleanroom procedures

Documentation

Education

Associate or B.S. in science or engineering

High School diploma

Tools

MS Office

Job description

Role

Manufacturing technician supporting cell therapy production, ensuring GMP compliance and cleanroom readiness.

Responsibilities

• Execute manufacturing steps per batch records, SOPs, and electronic instructions.
• Support equipment setup, material staging, and facility readiness.
• Monitor and operate processing equipment.
• Maintain documentation accuracy.
• Support deviation investigations, inventory control, and visual inspection activities.
• Collaborate across Manufacturing, Quality, Process Development, and other teams.

Requirements

• High School diploma with 2+ years GMP or technical experience, or associate/bachelor's in science or engineering with 0-2 years experience.
• Understanding of cGMP, aseptic techniques, cleanroom procedures.
• Ability to follow detailed instructions and escalated issues appropriately.

Preferred

• Experience in cell therapy, biologics, or biotech manufacturing.
• Familiarity with automated processing, batch record systems, and primary cell culture.
• Strong proficiency in MS Office.

High Value Skills

• Cell therapy, biologics, GMP manufacturing, cleanroom environment, process validation, deviation support, regulated documentation.

Work Setup

Salary range (~$82K-$123K), incentives, and benefits. Posted 14-Sep-2026, closing 18-Sep-2026.