Manufacturing Associate I - Second Shift

Immatics•Houston, TX

3d•Onsite

About The Position

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: Monday-Friday (On-Site); 1230-2100; (40 hours/week); Weekends/holidays as needed Department: CMC-GMP Reports to: Associate Manager, CMC-GMP Supervisory responsibilities: No Location: Manufacturing personnel alternate between the current office and manufacturing locations. Weatherford - 13203 Murphy Rd. Stafford, TX 77477 UTHealth Science Center- 1941 East Rd, BBSB 6102 Houston, TX 77054 Position Summary/objective: The primary purpose of this position is to perform complex, highly specialized and time sensitive technical cell manipulation and testing procedures on irreplaceable cellular products during clinical manufacturing.

Requirements

Bachelor’s Degree in Biology, Biochemistry, Biotechnology or other related field.
Zero (0) to Two (2) years of cell therapy manufacturing experience.
Legal eligibility to work in the United States is required.
Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment

Nice To Haves

Bachelor’s Degree in Biology, Biochemistry, Biotechnology or other related field.
One (1) to Two (2) years of cell therapy manufacturing experience.

Responsibilities

Knowledge of current cGMP.
Fulfill the operator and verifier roles in performing cell growth and manipulation procedures such as cell enrichment, cell culture, cellular product cryopreservation, cell product thaw/wash.
Accurately perform procedures in compliance with FDA’s Good Laboratory Practices, Good Manufacturing Practices, Good Tissue practices, as well as standards set by other accreditation agencies including but not limited to FACT, CAP, and CLIA.
Adhere to ALCOAC++ and cGDocP requirements while accurately performing procedures and maintaining documentation in compliance with SOPs.
Document deviations and events, notify supervisor and quality management personnel in timely manner, and assist in investigation of root cause and any required corrective actions.
Responsible for aseptic handling of reagents and products to ensure the integrity and sterility of cellular products until final infusion to the patient.
Must adhere to special cleaning and gowning requirements for the facility requiring specialized gowning such as masks, sterile jumpsuits, hair and shoe covers.
Ability to work productively and to participate in a highly creative and fast-paced environment.
Independently perform calculations to determine cell viability, dilutions, and cell concentrations.
Completes all appropriate logs and trackers.
Maintains GMP cleanliness: autoclaving, bleaching liquid waste, removing waste, general cleanliness and organization of the office and facility.
Maintains knowledge regarding donor evaluation, screening and testing, labeling and product acceptability and release criteria.
Conducts activities to support study plans, and IQ/OQ/PQs.
Provide input or feedback regarding change controls, WI, SOPs, study plans, reports, deviations, OOS/OOE, and CAPA’s as directed.
Performs routine equipment maintenance and troubleshooting.
Prepares and presents manufacturing summaries, as needed.