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Quality Control Analyst II

Immatics
United Statesfull_timeVerifiedPosted 8 Apr 2026

About the role

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. 

 
FLSA Classification: Non-Exempt/Hourly 

Schedule: Tuesday to Friday; (1st Shift 8:00 am – 6:30 pm) 

Department: Quality Control 

Reports to: Associate Quality Control Manager 

Supervisory responsibilities: No 

Locations: 13203 Murphy Road Stafford TX 77477  

Position Summary/objective:   

The main role of the Quality Control Analyst is to execute bio-analytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory.  

Essential functions: 

  • Perform release assays for cell product identity and safety, which includes the use of different laboratory methods such as microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma. 

  • Safely handle human biological specimens. 

  • Extract, compile, and analyze data.  

  • Generate, report, and track results. 

  • Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures. 

  • Travel from QC laboratory to manufacturing facility to perform visual inspections. 

  • Transport controlled documents between OQS office and QC laboratory. 

  • Transport QA-released QC materials between QC laboratories. 

  • Manage, in collaboration with other team members, supply inventory.  

  • Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, and release of materials and reagents. 

  • Perform routine equipment maintenance and troubleshooting. 

  • Maintain data integrity and logs for equipment.  

  • Assist with quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. 

  • Involved in the creation of systems used in quality control to maintain compliances with regulations 

 

Secondary Functions:  

  • Training junior analysts. 

  • Assist with equipment and assay qualifications and validations. 

Competencies: 

  • Initiative 

  • Problem Solving 

  • Very detail oriented 

  • Strong analytical, technical writing, verbal communication, and interpersonal skills 

  • Ability to work indep

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Company

Immatics

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