Advanced GMP Cellular Therapy Lab Tech II

Medical University of South Carolina; Town of Charleston (NY); On-site; USD 39,000 - 55,000; Full time

Job summary

The Medical University of South Carolina is seeking a GMP Lab Tech II to perform advanced cellular therapy manufacturing and laboratory operations in a regulated environment. You will execute complex cellular processing workflows, including isolation, expansion, enrichment, culture, cryopreservation, and quality control testing of human-derived products for clinical care and development.

This role supports end-to-end manufacturing, maintaining batch documentation, ensuring traceability, and

Qualifications

• Four-year college degree in medical technology or biological sciences.
• 2+ years clinical cell therapy experience.
• Basic hematology knowledge.
• Ability to learn new scientific theory and applications.
• Mature judgment and independent work with regular progress reviews.
• Strong teamwork and cross-functional collaboration.
• Ability to interpret data thoroughly and communicate findings.
• Strong math skills and attention to detail.
• Color vision screening is required.

Responsibilities

• Perform advanced cellular processing workflows in GMP environment.
• Maintain accurate batch documentation and product traceability.
• Apply flow cytometry and immunoassays for product characterization.
• Collaborate with clinical, laboratory, and quality teams.
• Support process development and SOP documentation.

Skills

Laboratory skills

Quality control

Data interpretation

Troubleshooting

Scientific writing

Team collaboration

Color vision

Education

Four-year college degree in medical technology or biological sciences

Master’s degree in medical sciences or related field

Tools

Flow cytometry

LIS software (Bluecord/Stemsoft)

Job description

The Medical University of South Carolina is seeking a GMP Lab Tech II to perform advanced cellular therapy manufacturing and laboratory operations in a regulated environment. You will execute complex cellular processing workflows, including isolation, expansion, enrichment, culture, cryopreservation, and quality control testing of human-derived products for clinical care and development.

This role supports end-to-end manufacturing, maintaining batch documentation, ensuring traceability, and