Quality Control Analyst I

Requirements

• 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
• In this r ole you w ill :
• 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
• Travel required: Less than 10%, domestically
• Wh at do we offer ?
• At Immatics , we believe in investing in our team 's health, safety and well-being . Here's what you can expect if you join Immatics :
• Comprehensive 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% e mployer- p aid l ife i nsurance up to at 1x annual salary , up to one hundred thousand dollars
• 100% e mployer -p aid s hort- and l ong-Term d isability c overage
• 401(k) with i mmediate e ligibility and company mat ch...
• The company will match 100% of your contributions up to 3% of your base salary for the first two years of employmen t , 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
• P artially paid p arental l eave for eligible employees.
• Additional voluntary employee - paid benefits and services, including a ccident , h ospital i ndemnity, and c ritical i llness insurance, as well as i dentity t heft p rotection and p et i nsurance .
• Equal Employment Opportunity
• Reasonable Accommodations
• We are committed to providing reasonable accommodations to individuals with disabilities and to appli

Benefits

Additional Information

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. Basic Qualification s : 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)

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