GMP Lab Tech II-3

United States·Charlestonmid

OtherTech

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Job Description SummaryThe GMP Lab Tech II performs advanced cellular therapy manufacturing and laboratory operations supporting clinical, translational,

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OtherTech

The GMP Lab Tech II performs advanced cellular therapy manufacturing and laboratory operations supporting clinical, translational, and investigational cell therapy programs within a highly regulated GMP environment. This role is responsible for the execution of complex cellular processing workflows, including cell isolation, expansion, enrichment, selection, culture, cryopreservation, and quality control testing of human-derived cellular products used in clinical care and therapeutic development.
The GMP Lab Tech II supports end-to-end manufacturing operations for advanced cellular therapies by performing aseptic processing activities within classified cleanroom environments, maintaining accurate batch documentation, and ensuring product traceability, compliance, and quality throughout the manufacturing lifecycle. The role applies specialized technical expertise in the processing of apheresis-derived products, immune cell populations, stem cell products, and emerging cellular therapies, while adhering to established cGMP, cGTP, biosafety, and contamination control requirements.
In collaboration with clinical, laboratory, research, and quality teams, the GMP Lab Tech II supports the development, optimization, validation, and implementation of novel cellular therapy manufacturing processes, including CAR-T, mesenchymal stem cell, dendritic cell, and other advanced therapeutic platforms. The role contributes to process improvement initiatives, equipment and procedure qualification activities, SOP development, and implementation of standardized workflows that enable the translation of innovative cellular therapies from research environments into clinical application.
The GMP Lab Tech II performs complex immunological, hematological, and cellular analyses to support product characterization, assay validation, and laboratory quality programs. Through advanced laboratory techniques including flow cytometry, ELISA-based assays, functional immune testing, and cellular analysis, this role evaluates product performance, investigates technical challenges, and generates data to support manufacturing decisions and continuous improvement.
The GMP Lab Tech II serves as a critical technical contributor within the cellular therapy program, bridging laboratory expertise, manufacturing execution, and quality oversight to support the safe, reliable, and compliant delivery of next-generation cellular therapies.

Medical University Hospital Authority (MUHA)

Employee

Regular

CC005736 CHS - CCT Lab

Hourly

Health-26

Education and Work Experience:

Four-year college degree with major in medical technology or biological sciences
2+ years clinical cell therapy experience
Basic hematology knowledge
Motivation and initiative to learn new scientific theory and applications
Mature judgment
Work independently with regular review of progress and results
Proven team player
Collaborate and communicate effectively across functions
Interpret data thoroughly
Strong trouble-shooting capabilities
Scientific writing skills, including preparation of clear, concise SOPs and technical reports
Strong math skills
Attention to detail
Must be able to differentiate between colors and pass a standardized color vision screen to perform this role

Requirements

~1 min read

Master’s college degree with a major in medical sciences or related field
Experience working within an academic cGMP laboratory, including familiarity with FDA and FACT accreditation requirements
Flow cytometry expertise
Immunotherapy experience
Cell selection operation experience (e.g., manual or CliniMACs)
Moderate LIS knowledge (e.g., Bluecord, Stemsoft)
A strong understanding of cGMP/cGTP standards

Education and Work Experience:

· Four-year college degree with major in medical technology or biological sciences

· 2+ years clinical cell therapy experience

· Basic hematology knowledge

· Motivation and initiative to learn new scientific theory and applications

· Mature judgment

· Work independently with regular review of progress and results

· Proven team player

· Collaborate and communicate effectively across functions

· Interpret data thoroughly

· Strong trouble-shooting capabilities

· Scientific writing skills, including preparation of clear, concise SOPs and technical reports

· Strong math skills

· Attention to detail

· Must be able to differentiate between colors and pass a standardized color vision screen to perform this role

Preferred Qualifications:

· Master’s college degree with a major in medical sciences or related field

· Experience working within an academic cGMP laboratory, including familiarity with FDA and FACT accreditation requirements

· Flow cytometry expertise

· Immunotherapy experience

· Cell selection operation experience (e.g., manual or CliniMACs)

· Moderate LIS knowledge (e.g., Bluecord, Stemsoft)

· A strong understanding of cGMP/cGTP standards

If you like working with energetic enthusiastic individuals, you will enjoy your career with us!

The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need.

Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees