Quality Control Analyst I

Immatics • Houston, TX

6d • Onsite

About The Position

Join Immatics and shape the future of cancer immunotherapy; one patient at a time! Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.

Why Join Us?
Innovative Environment: Help to pioneer advancements in cancer immunotherapy.
Collaborative Culture: Be part of a diverse team dedicated to your professional growth.
Global Impact: Contribute to therapies that make a lasting impact on patients globally.

Schedule: Tuesday to Friday; (8:00 am – 6:30 pm)
Reports to: Associate Quality Control Manager
Locations: 13203 Murphy Road, Suite 100, Stafford TX 77477

Role Overview: We are seeking a Quality Control (QC) Analyst to support product release testing within our QC laboratory. The QC Analyst will be responsible for executing bioanalytical, cell-based, and molecular assays to ensure product identity, safety, and quality in a GMP-regulated environment. This role also supports data analysis, documentation, and cross-functional quality processes to maintain compliance and operational excellence.

Requirements

• Bachelor’s degree in a scientific field (e.g., biology, biochemistry, or related discipline)
• 1+ years of experience in a GMP- or GxP-regulated laboratory environment
• Hands-on experience with cell culture and aseptic laboratory techniques
• Demonstrated experience executing and documenting assays in compliance with regulatory standards
• Experience supporting investigations, deviations, or quality systems processes (e.g., CAPA, OOS/OOE)

Nice To Haves

• Degree in biology, biochemistry, biomedical science/engineering, or a related discipline
• Experience with cell therapy, biologics, or GMP product release testing
• Proficiency in laboratory techniques such as flow cytometry, PCR, immunoassays, sterility, endotoxin, or mycoplasma testing
• Experience with cell-based potency assays and microbiological methods
• Familiarity with equipment qualification/validation and assay validation processes
• Proficiency in data analysis and documentation using tools such as Excel and other Microsoft Office applications
• Demonstrated ability to troubleshoot laboratory equipment and assays in regulated environments

Responsibilities

• Perform release testing using bioanalytical, cell-based, and molecular methods to assess product identity, safety, and quality
• Execute laboratory assays (e.g., cell culture, flow cytometry, PCR, sterility, endotoxin) and analyze resulting data
• Maintain accurate, compliant documentation in accordance with cGMP/GxP and data integrity standards
• Support investigations, deviations, CAPAs, and other quality system activities
• Perform routine equipment maintenance, calibration support, and troubleshooting
• Collaborate cross-functionally to support material management, inspections, and laboratory operations
• Assist with assay validation, training of junior staff, and continuous improvement of QC processes

Benefits

• Competitive rates for Health, Dental, and Vision Insurance
• 4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
• 12 company paid holidays
• 7 days of sick time
• 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars
• 100% employer-paid short- and long-Term disability coverage
• 401(k) with immediate eligibility and company match
• Partially paid parental leave for eligible employees.
• Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level