Quality Control Analyst II

Immatics; Georgia; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Vacation: 4 weeks

Federal holidays: 12 days

Life insurance

disability coverage

401(k) with company match

Job summary

Immatics is hiring 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 lab, with a schedule of 12:30 PM - 11:00 PM, Monday to Thursday, on-site at Stafford, TX.

You will perform release assays, handle human specimens, analyze data, and ensure compliance with cGMP/GxP. Ideal candidates have a science degree and 2+ years in a regulated lab environment.

Qualifications

• BA or BS in any science-related field; minimum two years in a regulated lab.
• Preferred: Biology or related bioscience degree; strong lab skills in multiple assays.
• Experience with regulatory requirements (cGMP/GxP) is expected.

Responsibilities

• Perform release assays for cell product identity and safety using various lab methods.
• Safely handle human biological specimens.
• Extract, compile, and analyze data.
• Generate, report, and track results.
• Follow cGMP/GxP, regulatory filings and SOPs; document activities.
• Transport controlled documents between OQS and QC labs; move QC materials between labs.
• Collaborate to manage supply inventory.

Skills

Visual inspection

Cell count & viability

Flow cytometry

Cell culture

Immunoassays

DNA isolation

PCR

Sterility

Endotoxin

Mycoplasma

Cell Based Potency Assays

LIMS experience

Education

BA or BS in any science-related field

BA or BS in Biology/ Biological Sciences/ Laboratory Science/ Biochemistry/ Biomedical Science/Engineering

Tools

LIMS

Job description

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 II to support our Global Quality Operations team. The QC Analyst II will be responsible for executing bioanalytical, cell-based, and/or molecular methods for product release in the Quality Control laboratory.

Schedule : 12:30 PM - 11:00 PM; Monday to Thursday; On-site

Reports to : Associate Quality Control Manager

Location : 13203 Murphy Road Suite 100 Stafford, TX 77477

Basic Qualifications:

• BA or BS in any science-related field.
• Minimum two (2) years' experience in a regulated laboratory environment.

Preferred Qualifications:

• BA or BS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering
• Laboratory skills including any of the following: Visual inspection, cell count & viability, flow cytometry, cell culture, immunoassays, DNA isolation, PCR, sterility, endotoxin, and mycoplasma
• Cell Based Potency Assays
• Experience with LIMS

In this role you will:

• Perform release assays for cell product identity and safety, which includes the use of different laboratory methods such as 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
• Transport controlled documents between OQS office and QC laboratory
• Transport QA-released QC materials between QC laboratories
• Manage, in collaborations with other team members, supply inventory

Qualified candidates will participate in a structured interview process, which includes:

• An initial recruiter phone screen (conducted via video)
• Interviews with the hiring leader and other key stakeholders (via video)
• A final-stage interview

What do we offer?

At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics

Comprehensive 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. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary 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.

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, marital status, disability, genetic information, veteran status, or any other status protected by applicable law.

Reasonable Accommodations

We are committed to providing reasonable accommodations to individuals with disabilities and to applicants with sincerely held religious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us at [e-mail] .

Work Authorization

Applicants must be authorized to work in the United States without the need for current or future sponsorship.

Pre-Employment Requirements

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, wher