Senior Manufacturing Associate

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. 

Role Overview 

We are seeking a Senior Manufacturing Associate to support our CMC-GMP Manufacturing team. In this role, you will lead and execute complex, time-sensitive cell processing and testing activities for patient-derived cellular products in a clinical manufacturing environment. You will be responsible for ensuring compliance with GMP standards, maintaining product integrity and sterility, and overseeing accurate documentation and batch execution. As a senior team member, you will also provide technical guidance, support process improvements, and contribute to maintaining high operational standards across manufacturing activities. 

  
Schedule: 0700 – 1530; Monday to Friday 
Reports to: Manufacturing Manager  
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477 

Basic Qualifications:  

• Associate’s or Bachelor’s degree in a scientific field (e.g., biology, biotechnology, or related discipline)  

• 4+ years of experience in GMP-regulated manufacturing, preferably in cell therapy or biologics  

• Demonstrated experience executing aseptic processing and working in cleanroom environments (Grade A–D)  

• Proven ability to maintain compliant documentation in accordance with ALCOA++ and cGDocP standards  

• Experience identifying deviations and supporting investigations, CAPAs, and quality systems 

Preferred Qualifications:  

• Bachelor’s degree in a scientific field 

• Experience in cell therapy manufacturing, including cell culture, cryopreservation, and cell processing techniques  

• Familiarity with GLP, GTP, and industry standards (e.g., FACT, CAP, CLIA)  

• Experience supporting validation activities (IQ/OQ/PQ) and change control processes  

• Advanced troubleshooting skills and ability to resolve complex manufacturing or equipment issues  

• Experience mentoring or training junior staff and contributing to team development  

• Demonstrated ability to drive process improvements in a GMP-regulated environment 

In this role you will:  

• Execute and verify cell processing activities, including cell culture, enrichment, cryopreservation, thawing, and washing  

• Perform manufacturing operations in compliance with GMP, GLP, GTP, and applicable regulatory standards  

• Maintain accurate, compliant documentation and batch records in line with ALCOA++ and cGDocP requirements  

• Ensure aseptic handling and cleanroom compliance to maintain product sterility and integrity  

• Identify, document, and support investigation of deviations, including CAPA implementation  

• Perform calculations, equipment maintenance, and routine manufacturing support activities  

• Lead manufacturing runs, mentor junior team members, and contribute to continuous improvement initiatives 

What 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