QC Analyst II — Evening Shift, Bio/Lab

Immatics US, Inc.

Houston (TX)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Health Insurance
Dental Insurance
Vision Insurance
Vacation
Holidays
Sick time
Life Insurance
Disability Insurance
401(k) Matching
Parental Leave
Voluntary benefits

Job summary

Immatics US, Inc. in Stafford, TX is seeking a Quality Control Analyst II to support our Global Quality Operations team. You will execute bioanalytical, cell-based, and molecular methods for product release in the QC laboratory.

Schedule: 12:30 PM – 11:00 PM, Monday to Thursday, On-site. The role requires a BA/BS in science and at least two years in a regulated lab, with experience in flow cytometry, PCR, immunoassays, and cGMP/GxP.

Qualifications

  • BA or BS in a science-related field and at least 2 years in a regulated lab.
  • Experience performing bioanalytical, cell-based, or molecular methods for product release.
  • Knowledge of cGMP/GxP and regulatory documentation.

Responsibilities

  • Perform release assays for cell product identity and safety using multiple lab methods.
  • Safely handle human biological specimens.
  • Extract, compile, and analyze data.
  • Generate, report, and track results.
  • Conduct activities consistent with cGMP/GxP and regulatory filings.
  • Transport controlled documents between OQS and QC labs; transport QA-released QC materials.
  • Manage, in collaboration with team, supply inventory.
  • Travel less than 10%.

Skills

Visual inspection
Cell count & viability
Flow cytometry
Cell culture
Immunoassays
DNA isolation
PCR
Sterility
Endotoxin
Mycoplasma

Education

BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering
BA or BS in any science-related field

Tools

LIMS

Job description

Immatics US, Inc. in Stafford, TX is seeking a Quality Control Analyst II to support our Global Quality Operations team. You will execute bioanalytical, cell-based, and molecular methods for product release in the QC laboratory.

Schedule: 12:30 PM – 11:00 PM, Monday to Thursday, On-site. The role requires a BA/BS in science and at least two years in a regulated lab, with experience in flow cytometry, PCR, immunoassays, and cGMP/GxP.

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