Quality Control Analyst II (1073)

Join Immatics and shape the future of cancer immunotherapy; one patient at a time!  

Immatics is at the forefront of immunotherapy innovation, working to harness the power of T cells to transform cancer treatment.  

Immatics is an exceptional clinical-stage biopharmaceutical company active in the discovery and development of T cells redirecting cancer immunotherapies. We use these powerful T cells to develop groundbreaking immunotherapies that target cancer cells. We are dedicated to transforming cancer treatment and improving patient outcomes through cutting-edge research and advanced TCR technology. 

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. 

We are seeking an QC Analyst II to support our Quality Control team. The QC Analyst II primary responsibilities to support the company’s ongoing clinical trials by performing complex, highly specialized, and time sensitive technical cell manipulation and/or analytical tests to characterize and assess the functionality of final products. This position will work with the current process and Analytical Development teams, facilitating coordination among personnel and providing technical input to facilitate clinical and non-clinical assays. 

FLSA Classification: Hourly, Non-Exempt  
Schedule: 8:00 AM – 4:30 PM; Monday to Friday; On-site  
Reports to: Associate QC Manager  
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477  

What You’ll Do: 

As an QC Analyst II, you will play a key role in supporting our quality control operations:  

• Work under minimum supervision. 

• Assist with Qualification and Validation of QC assays. 

• Assist with the installation and validation of sophisticated laboratory instrumentation and computer systems to collect and record data. 

• Perform advanced assays requiring precise analytical skills and understanding of microbiology and molecular/cell biology principles. 

• Investigate deviations and out of specifications. 

• Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality. 

• Contribute to writing and revising Standard Operating Procedures (SOPs), Technical Reports, and other Good Manufacturing Practices (GMP) documentation as appropriate. 

• Maintain data integrity and compliance with company SOPs and specifications, FDA,