Job Description

JoinImmaticsandshape thefuture ofcancerimmunotherapy; one patient at atime!

Immaticsis 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. Ourcutting-edgescience and robust clinical pipeline form the broadest PRAMEfranchise with the most PRAMEindications and modalities, spanning TCR T-cell therapies and TCRbispecifics

Why Join Us?

• Innovative Environment:Help topioneeradvancementsin cancer immunotherapy.

• Collaborative Culture:Be part of a diverse team dedicated to your professionalgrowth.

• Global Impact:Contribute to therapies thatmakealasting impactonpatientsglobally

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 willbe responsible forensuring compliance with GMP standards,maintainingproduct integrity and sterility, and overseeingaccuratedocumentation and batch execution. As a senior team member, you will alsoprovidetechnical guidance, support process improvements, and contribute tomaintaininghigh operational standards across manufacturing activities.

 
Schedule1430–2300; Monday to Friday
Reports toManufacturing Manager 
Location 13203Murphy Road Suite 100 Stafford, TX 77477

Basic Qualifications

• Associate’s or Bachelor’sdegree 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 tomaintaincompliant documentationin accordance withALCOA++ andcGDocPstandards

• Experienceidentifyingdeviations and supporting investigations, CAPAs, and quality systems

PreferredQualifications

• 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 thisrole youwill

• 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

• Maintainaccurate, compliant documentation and batch records in line with ALCOA++ andcGDocPrequirements

• Ensure aseptic handling and cleanroom compliance tomaintainproduct 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

What do we offer? 

AtImmatics, we believe in investing in our team’s health,safetyand well-beingHere’swhat you can expectif youjoinImmatics

Comprehensive Benefits 

• Competitive rates forHealth, Dental, and Vision Insurance

• 4 weeks ofvacation,granted up front each year and prorated for firstand lastyear ofemployment.

• 12 company paid holidays

• 7daysof sick time

• 100%employer-paidlifeinsurance up toat 1x annual salary, up to one hundred thousand dollars

• 100%employer-paidshort- andlong-Termdisabilitycoverage 

• 401(k) withimmediateeligibility andcompany match…

• The company will match100% of your contributions upto3% of yourbase salaryfor the first two yearsof employment, 4% foryears 2-3 of employment, and up to5%of your salaryfrom the fourth year onward of continued employment.

• Partiallypaidparentalleave for eligible employees.

• Additionalvoluntary employee-paidbenefits and services,includingaccident,hospitalindemnity, andcriticalillnessinsurance, as well as identitytheftprotection andpetinsurance

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplaceWe consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.

ReasonableAccommodations

We are committed to providing reasonableaccommodationsto individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observancesIf yourequireassistanceoraccommodationduring theapplicationor interview process, please contact us atPRIOR:

Work authorization/security clearance requirements

Legal eligibility to work in the United States isrequiredImmaticsparticipates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment  

 Affirmative Action/EEO statement

Immaticsis an equalopportunityemployer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs.