Senior Manufacturing Associate

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 ofPRAME a target expressed in more than 50 cancers. Ourcutting-edgescience and robust clinical pipeline form the broadestPRAMEfranchise with the mostPRAMEindications and modalities spanning TCR T-cell therapies and TCRbispecifics.

Why Join Us

• Innovative Environment:Help topioneeradvancementsin cancer immunotherapy.

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

• Global Impact:Contribute to therapies thatmakealasting impactonpatientsglobally.

Role Overview

We are seeking a Senior Manufacturing Associate to support our CMC-GMP Manufacturing 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 standardsmaintainingproduct 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.

Schedule:; Monday to Friday
Reports to:ManufacturingManager
Location: 13203Murphy Road Suite 100 Stafford TX 77477

Basic Qualifications:

• Associates or Bachelorsdegree 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 AD)

• Proven ability tomaintaincompliant documentationin accordance withALCOA andcGDocPstandards

• Experienceidentifyingdeviations and supporting investigations CAPAs and quality systems

PreferredQualifications:

• Bachelors 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 teams healthsafetyand you can expectif youjoinImmatics:

Comprehensive Benefits:

• Competitive rates forHealth Dental and Vision Insurance

• 4 weeks ofvacationgranted up front each year and prorated for firstand lastyear ofemployment.

• 12 company paid holidays

• 7daysof sick time

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

• 100%employer-paidshort- andlong-Termdisabilitycoverage

• 401(k) withimmediateeligibilityandcompany 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.

• Partiallypaidparentalleavefor eligible employees.

• Additionalvoluntary employee-paidbenefits and servicesincludingaccidenthospitalindemnity andcriticalillnessinsurance as well as identitytheftprotection andpetinsurance.

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We 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.

Reasonable Accommodations

We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs practices or observances. If you require assistance or accommodation during the application or interview process please contact us at.

Work Authorization

Applicants mustbe authorized towork in the United States without the need for current or future sponsorship. Visa sponsorships may beavailablefor certain roles.

Pre-Employment Requirements

Employment is contingent upon successful completion of a background check referencechecksand pre-employment drug screening wherepermittedby applicable law. For certain rolesadditionalscreenings such as a credit check or motor vehicle record review may berequired where job-related and consistent with business necessity.