Director, Facilities, Engineering, and Maintenance
ImmaticsAbout 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.
Role Overview:
Immatics is seeking an experienced Director of Facilities, Engineering & Maintenance to lead the infrastructure and engineering operations that power our next-generation cell therapy manufacturing environments. This role is instrumental in ensuring our highly specialized GMP facilities can support clinical manufacturing, operational scalability, and future commercial readiness for innovative cancer immunotherapies. The ideal candidate combines deep technical expertise in regulated biopharmaceutical operations with strong leadership, operational excellence, and the ability to scale complex infrastructure in a high-growth environment.
Reports to: Chief Operating Officer
Location: 13203 Murphy Road, Suite 100, Stafford, TX 77477
Basic Qualifications:
Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, or related field)
10+ years of experience in facilities engineering and maintenance within biotech, pharmaceutical, or other GMP-regulated environments
5+ years of leadership experience managing engineering or facility operations teams
Demonstrated experience leading GMP facility projects (e.g., startup, expansion, or upgrades) and managing critical utilities and cleanroom operations
Proven experience ensuring compliance with GMP regulations, audits/inspections, and managing external contractors and capital projects
Preferred Qualifications:
Master’s degree in Engineering, Facilities Management, or a related discipline
Experience in commercial-stage cGMP manufacturing environments
Experience in cell therapy, biologics, or advanced therapy medicinal products (ATMPs)
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