Quality Control Analyst II: Cell & Bioassay Release

Immatics; Stafford (TX); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Health Insurance

Vacation

Sick Time

Life Insurance

Disability

401(k) match

Parental Leave

Additional benefits

Job summary

Immatics is seeking a Quality Control Analyst II to support Global Quality Operations in Stafford, TX. The role involves executing bioanalytical, cell-based, and molecular methods for product release in the QC lab, with on-site schedule 12:30 PM – 11:00 PM, Monday to Thursday.

The ideal candidate has a BA/BS in a science field and at least two years in a regulated lab, with familiarity in cGMP/GxP and data documentation. Join a team advancing cancer immunotherapy.

Qualifications

• BA or BS in a science field and at least two years in a regulated laboratory environment.
• Experience with cGMP/GxP and rigorous data documentation is preferred.
• Strong analytical and communication skills in a regulated setting.

Responsibilities

• Perform release assays for cell product identity and safety using multiple laboratory methods.
• Safely handle human biological specimens.
• Extract, compile, and analyze data from experiments.
• Generate, report, and track results in the QC system.
• Maintain documentation in line with cGMP/GxP and regulatory filings.
• Transfer controlled documents between OQS and QC laboratories.
• Collaborate to manage supply inventory with teammates.

Skills

Cell counting

Flow cytometry

Cell culture

Immunoassays

DNA isolation

PCR

Sterility

Endotoxin

Mycoplasma

cGMP/GxP

Education

BA/BS in science field

Biology/Biomedical science background

Tools

LIMS

Job description

Immatics is seeking a Quality Control Analyst II to support Global Quality Operations in Stafford, TX. The role involves executing bioanalytical, cell-based, and molecular methods for product release in the QC lab, with on-site schedule 12:30 PM – 11:00 PM, Monday to Thursday.

The ideal candidate has a BA/BS in a science field and at least two years in a regulated lab, with familiarity in cGMP/GxP and data documentation. Join a team advancing cancer immunotherapy.