Operational Quality Systems Specialist I

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 Operational Quality Systems Specialist I to provide support to the Operational Quality Systems team by guidance and oversight on tasks related to training and document control.  

FLSA Classification: Hourly, Non-Exempt  
Schedule: 8:00 AM – 5:00 PM; Monday to Friday; On-site  
Reports to: Associate Manager, Operational Quality Systems   
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477  

What You’ll Do: 

As an Operational Quality Systems Specialist I, you will play a key role in supporting our Operational Quality Systems:  

• Responsible for maintaining the existing quality system while ensuring compliance with applicable policies, procedures, and regulatory requirements.   

• Instrumental in improving the quality system as applicable.   

• May lead quality system projects, audit readiness activities, improvements or initiatives and collaborate with site operations and engineering teams.  

• Monitor and review Quality Management Systems (Quality Systems, Audits, CAPA, Complaints, Document Control, Training, Metrics) and Batch Record Issuance procedures to ensure and maintain compliance with corporate and regulatory agency requirements  

• Contribute to the writing, coordination, review, approval and maintenance of the OQS Procedures and documents.  

• Coordinate, support, and investigate Corrective and Preventive Actions (CAPAs).   

• Perform quality metrics/key performance indicators (KPIs) to track compliance performance and analyze data to implement improvements and streamline processes and procedures.   

• Maintain and manage