Quality Control Analyst II
ImmaticsAbout the role
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.
FLSA Classification: Non-Exempt/Hourly
Schedule: Tuesday to Friday; (1st Shift 8:00 am – 6:30 pm)
Department: Quality Control
Reports to: Associate Quality Control Manager
Supervisory responsibilities: No
Locations: 13203 Murphy Road Stafford TX 77477
Position Summary/objective:
The main role of the Quality Control Analyst is to execute bio-analytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory.
Essential functions:
Perform release assays for cell product identity and safety, which includes the use of different laboratory methods such as microscopy, visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma.
Safely handle human biological specimens.
Extract, compile, and analyze data.
Generate, report, and track results.
Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures.
Travel from QC laboratory to manufacturing facility to perform visual inspections.
Transport controlled documents between OQS office and QC laboratory.
Transport QA-released QC materials between QC laboratories.
Manage, in collaboration with other team members, supply inventory.
Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, and release of materials and reagents.
Perform routine equipment maintenance and troubleshooting.
Maintain data integrity and logs for equipment.
Assist with quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc.
Involved in the creation of systems used in quality control to maintain compliances with regulations
Secondary Functions:
Training junior analysts.
Assist with equipment and assay qualifications and validations.
Competencies:
Initiative
Problem Solving
Very detail oriented
Strong analytical, technical writing, verbal communication, and interpersonal skills
Ability to work indep
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s