Senior Manufacturing Associate - Second Shift

Requirements

• 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 r ole you w ill :
• 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
• Wh at 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 up front each year and prorated for first and last year of employment.
• 12 company paid holidays
• 7 days of sick time
• 100% e mployer- p aid l ife i nsurance up to at 1x annual salary , up to one hundred thousand dollars
• 100% e mployer -p aid s hort- and l ong-Term d isability c overage
• 401(k) with i mmediate e ligibility and company mat ch...
• The company will match 100% of your contributions up to 3% of your base salary for the first two years of employmen t , 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
• P artially paid p arental l eave for eligible employees.
• Additional voluntary employee - paid benefits and services, including a ccident , h ospital i ndemnity, and c ritical i llness insurance, as well as i dentity t heft p rotection and p et i nsurance .
• Equal Employment Opportunity

Benefits

Additional Information

J oin Immatics and s hape the f uture of c ancer i mmunotherapy ; 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 patient s 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 : 143 0 - 23 00; Monday to Frida y Reports to : Manufacturing Manager Location : 1320 3 Murphy Road Suite 100 Stafford, TX 77477 Basic Qualification s : 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

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