Quality Control Analyst II

Immatics • Houston, TX

5d • Onsite

About The Position

Immatics is seeking a Quality Control Analyst II to support its Global Quality Operations team. The role executes bioanalytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory, including release assays for cell product identity and safety. The position is onsite in Stafford, Texas, and works Monday through Thursday from 12:30 PM to 11:00 PM. It reports to the Associate Quality Control Manager, with travel requirements of less than 10% and described as minimal.

The analyst safely handles human biological specimens; extracts, compiles, analyzes, reports, and tracks data and results; and documents work in accordance with cGMP/GxP, regulatory filings, and written procedures. The role also transports controlled documents and QA-released QC materials between designated offices and laboratories and manages supply inventory in collaboration with team members. Applicants must be authorized to work in the United States without current or future sponsorship. Employment is contingent on applicable pre-employment checks.

Requirements

• BA or BS in a science-related field.
• At least two years of experience in a regulated laboratory environment.
• Authorization to work in the United States without the need for current or future sponsorship.

Nice To Haves

• BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering.
• Laboratory skills in one or more of the following: visual inspection, cell count and viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, or mycoplasma.
• Experience with cell-based potency assays.
• Experience with LIMS.

Responsibilities

• Perform release assays for cell product identity and safety using applicable laboratory methods.
• Safely handle human biological specimens.
• Extract, compile, and analyze data.
• Generate, report, and track results.
• Conduct and document activities consistent with cGMP/GxP, regulatory filings, and written procedures.
• Transport controlled documents between the OQS office and QC laboratory.
• Transport QA-released QC materials between QC laboratories.
• Manage supply inventory in collaboration with other team members.

Benefits

• Health, dental, and vision insurance at competitive rates.
• Four weeks of vacation granted up front each year, prorated for the first and last year of employment.
• 12 company-paid holidays.
• Seven days of sick time.
• Employer-paid life insurance equal to 1x annual salary, up to $100,000.
• Employer-paid short- and long-term disability coverage.
• 401(k) with immediate eligibility and a company match.
• Partially paid parental leave for eligible employees.
• Optional employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, identity theft protection, and pet insurance.

What This Job Offers

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