Materials Management and Logistics Specialist II

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 a Materials Management and Logistics Specialist II to support our US Facilites and Operations team. This position is intended to provide on-the-floor daily support for GMP and non-GMP warehouse.  This role will be responsible for maintaining daily operations in the GMP warehouse, providing support for materials inside classified cleanroom spaces and to internal customers. 

FLSA Classification: Hourly, Non-Exempt  
Schedule: 2:00 PM – 10:30 PM; Monday to Friday; On-site  
Reports to: Senior Manager, Materials Management and Logistics  
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477  

What You’ll Do: 

As a Materials Management and Logistics Specialist II support day to day operations of the GMP and non-GMP warehouses including:  

• Supports the GMP Manufacturing team by preparing necessary materials for manufacturing use.  

• Receive, evaluate and disposition GMP and non-GMP materials. 

• Timely receipt of biologic materials, i.e. patient starting material (fresh or cryopreserved leukapheresis). 

• Maintain GMP/non-GMP inventory via cycle counts and electronic inventory controls. 

• Maintain receiving log by adhering to established Work Instructions/SOPs. 

• Accurately and aseptically perform material kitting per established pick lists according to the manufacturing calendar.  

• Successfully complete aseptic gowning qualification and maintain qualified status.  

• Transfer kitted materials into appropriate manufacturing locations.  

• Ensure materials are appropriately disinfected and ready for aseptic use.  

• Adhere to manufacturing production schedule to maintain material readiness. 

• Identify and resolve any discrepancies between picked materials and actual materials used.  

• Timely transfer of cryogenic products, i.e. Final Drug Products, to liquid nitrogen storage. 

• Packout of final drug product for delivery to global clinical sites. 

• Maintain accurate documentation in compliance with FDA’s Good Laboratory Practices, Good Documentation Practices, Good Manufacturing Practices, Good Tissue Practices, as well as standards set by other accreditation agencies including but not limited to FACT, CAP, and CLIA.   

• Adhere to ALCOA++ and cGDocP requirements while accurately performing procedures and maintaining documentation in compliance with SOPs. 

• Notify supervisor and quality management of any deviations and events. Assist in investigati