Senior CMC Program Manager

## Senior CMC Program Manager Apply:
Houston:
Full time:
Posted Yesterday:
JR100761
*** 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 Program Manager, CMC to lead and coordinate cross-functional Chemistry, Manufacturing, and Controls (CMC) activities within a cell therapy development and manufacturing environment. The Senior Program Manager, CMC will drive planning, execution, and integration across manufacturing, analytical, quality, regulatory, and supply chain functions to support clinical development and commercialization goals. This role serves as a strategic partner across technical and operational teams, ensuring alignment, proactive risk management, and readiness for key milestones, including regulatory submissions and commercial manufacturing.

** Reports to**:
Senior Director, Program Management  
** Location**: 13203 Murphy Road Suite 100 Stafford, TX 77477   
*
* Basic Qualifications:

*** Bachelor's degree in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
* 7 years of experience within biotechnology, pharmaceutical, or oncology-focused clinical development environments
* Demonstrated experience in CMC program/project management or complex project leadership, leading cross-functional CMC activities, including manufacturing, quality, analytical, and regulatory operations
* Academic or industry experience in cell and gene therapy, immunology/oncology, or bioprocessing/manufacturing sciences  
*
* Preferred Qualifications:

*** Advanced degree such as a Masters or PhD in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
* Experience supporting late-stage CMC programs in immunology, oncology, or cell and gene therapy
* Proven experience managing complex programs and critical paths across multiple technical and operational functions
* Proficiency with project management tools, dashboards, and reporting systems in regulated environments
* Proven leadership, stakeholder management, and organizational skills with the ability to manage competing priorities in fast-paced environments
* Advanced ability to identify risks, drive decision-making, and implement process improvements across cross-functional teams
* Experience coordinating external vendors, CMOs, CDMOs, or consulting partners
* Strong communication and presentation skills with experience supporting senior leadership discussions and strategic planning  
** In this role you will:
*** Develop and maintain CMC program plans, timelines, risk registers, trackers, and reporting tools to support integrated program execution
* Manage CMC deliverables, milestones, and critical paths while ensuring alignment with overarching development program timelines
* Lead and facilitate cross-functional CMC meetings, including agenda development, documentation, action tracking, and follow-up activities
* Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality, Regulatory, Supply Chain,…