Manufacturing Associate II

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.

About the Role

We are seeking a Manufacturing Associate II to support our CMC-GMP team. The Manufacturing Associate II will be responsible for performing complex, highly specialized and time-sensitive technical cell manipulations and testing procedures on irreplaceable cellular products during clinical manufacturing.

Location: 13203 Murphy Road Suite 100, Stafford, TX 77477
Reports to: Associate Manufacturing Manager

Schedule

• 2:30 PM – 11:00 PM
• Monday to Friday
• On-site

Qualifications

Basic Qualifications

• Biomanufacturing Technology Associate of Applied Science Degree, Biomanufacturing Technology Level 2 Certificate, or equivalent or Associate degree in biology, Biochemistry, Biotechnology, Biomanufacturing, or other related field.
• 2+ years of cell therapy manufacturing experience.

Preferred Qualifications

• Bachelor's degree in biology, Biochemistry, Biotechnology, or another related field.

Responsibilities

• Fulfill the operator and verifier roles in performing cell growth and manipulation procedures such as cell enrichment, cell culture, cellular product cryopreservation, and 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 a timely manner, and assist in the 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.
• Adhere to special cleaning and gowning requirements for the facility, including specialized gowning such as masks, sterile jumpsuits, hair, and shoe covers.
• Work productively and participate in a highly creative and fast-paced environment.
• Independently perform calculations to determine cell viability, dilutions, and cell concentrations.

Benefits

• Comprehensive health, dental, and vision insurance at competitive rates.
• 4 weeks of vacation, granted up front each year and prorated for the first and last year of employment.
• 12 company-paid holidays.
• 7 days of sick time.
• 100% employer-paid life insurance up to 1x annual salary (up to $100,000).
• 100% employer-paid short- and long-term disability coverage.
• 401(k) with immediate eligibility and company match:
  • 100% match up to 3% of base salary for the first two years of employment.
  • 4% match for years 2-3 of employment.
  • Up to 5% match from the fourth year onward of continued employment.
• Partially paid parental leave for eligible employees.
• Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.

Applicants must be authorized to work in the United States without the need for current or future sponsorship. Employment is contingent upon successful completion of a background check, reference checks, and pre-employment drug screening, where permitted by applicable law. For certain roles, additional screenings such as a credit check or motor vehicle record review may be required, where job-related and consistent with business necessity.