QC Specialist I — Cell Therapy Manufacturing (Houston)

Kids for the Future; Houston (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

CTMC, a pioneering biotech joint venture in Houston, seeks a Quality Control professional to support daily QC operations including in-process and finished product analysis, stability samples, and environmental monitoring.

The role requires a Bachelor’s in Biological Sciences and at least 1 year in aseptic manufacturing (cell and gene therapy), with knowledge of cGMP and FDA regulations. You will work in GMP areas, collaborating with supervisors and teams to maintain quality and compliance.

Qualifications

• Bachelor’s degree in Biological Sciences, Biotechnology or related field.
• 1+ year in aseptic manufacturing (cell and gene therapy).
• Knowledge of cGMP and FDA regulations.
• Experience with non-conformances or laboratory investigations is a plus.

Responsibilities

• Support day-to-day QC functions and analyze in-process and finish products.
• Demonstrate aseptic processing capability for tests.
• Participate in assay transfer and qualification studies.
• Perform sterility, growth promotion and pH testing.
• Conduct Environmental Monitoring in GMP areas.
• Generate trend analyses for environmental data.
• Assist in SOPs and equipment qualification documents.
• Collaborate with other departments to ensure timely testing.
• Oversee QC laboratory functions and maintenance of equipment.

Skills

Aseptic manufacturing

cGMP knowledge

Laboratory analyses

Communication skills

Planning & organization

Education

Bachelor’s degree in Biological Sciences

Job description

CTMC, a pioneering biotech joint venture in Houston, seeks a Quality Control professional to support daily QC operations including in-process and finished product analysis, stability samples, and environmental monitoring.

The role requires a Bachelor’s in Biological Sciences and at least 1 year in aseptic manufacturing (cell and gene therapy), with knowledge of cGMP and FDA regulations. You will work in GMP areas, collaborating with supervisors and teams to maintain quality and compliance.