Quality Control Analyst I

Immatics • Houston, TX

5d • 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.

Role Overview
We are seeking a Quality Control Analyst I to support our Global Quality Operations Team. The Quality Control Analyst I will be responsible for The main role of the Quality Control Analyst I is to execute bio-analytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory.

Requirements

• Bachelor’s degree in a life sciences-related discipline.
• Strong attention to detail with a high level of accuracy in documentation and data review.
• Demonstrated ability to take initiative and work independently in a fast-paced environment.
• Effective problem-solving and critical-thinking skills.
• Ability to follow written procedures and maintain compliance with quality and regulatory standards.
• Applicants must be authorized to work in the United States without the need for current or future sponsorship.

Nice To Haves

• Bachelor’s degree in Biology, Biological Sciences, Laboratory Science, Biochemistry, Biomedical Science, or Biomedical Engineering.
• Hands-on laboratory experience in a regulated or research environment.
• Familiarity with cellular manufacturing, process development, or related biological and biochemical applications.
• Working knowledge of laboratory techniques and analytical testing methods.
• Experience handling and documenting biological samples in accordance with cGMP/GxP standards.
• Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint.
• Strong organizational, communication, and data analysis skills.

Responsibilities

• 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.
• 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

Benefits

• Competitive rates for Health, Dental, and Vision Insurance
• 4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
• 12 company paid holidays
• 7 days of sick time
• 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars
• 100% employer-paid short- and long-Term disability coverage
• 401(k) with immediate eligibility and company match
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level