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Quality Control Biotechnology Jobs in Texas (NOW HIRING)

Radiomedix, Inc.

Quality Control Chemist II

Humble, TX · On-site

Must have at least 2-3 years of QC experience in biotech, pharma, or cGMP * Conducts analytical/quality control testing in accordance with cGMP (21 CFR 211) for API and Drug products to ensure safety ...

Radiomedix, Inc.

Quality Control Chemist II

Humble, TX · On-site

Must have at least 2-3 years of QC experience in biotech, pharma, or cGMP * Conducts analytical/quality control testing in accordance with cGMP (21 CFR 211) for API and Drug products to ensure safety ...

IJC-HRS staffing

Be Seen First

QA QC Inspector

Houston, TX · On-site

$70 - $75/hr

This is a hands-on QA/QC position inspecting fabricated piping systems, orbital GTAW (TIG) welds ... Experience supporting fabrication for semiconductor, pharmaceutical, food & beverage, biotechnology ...

NTG Staffing

EM Tech II

The Woodlands, TX

$28/hr

Works in a fast-paced environment supporting the quality control department of a CMDO for ... the biotech, pharmaceutical, or cell/gene therapy industries. Have the knowledge and ability to ...

NTG Staffing

EM Tech II

The Woodlands, TX · On-site

$28/hr

Works in a fast-paced environment supporting the quality control department of a CMDO for ... biotech, pharmaceutical, or cell/gene therapy industries. • Have the knowledge and ability to ...

Charles River Laboratories, Inc.

... change control, and internal audit activities. • Communicate all identified quality and ... Our client base includes global pharmaceutical companies, biotechnology companies, government ...

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Quality Control Biotechnology information

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$12

$19

$27

How much do quality control biotechnology jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for quality control biotechnology in Texas is $19.53, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $21.49 per hour, depending on experience, location, and employer.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What are the key skills and qualifications needed to thrive as a quality control biotechnology professional?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

What does quality control do in biotechnology?

In biotechnology, quality control involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP and ISO standards.

What is the difference between Quality Control Biotechnology vs Quality Assurance Biotechnology?

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

What are popular job titles related to Quality Control Biotechnology jobs in Texas? For Quality Control Biotechnology jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Quality Control Biotechnology jobs in Texas look for? The top searched job categories for Quality Control Biotechnology jobs in Texas are:
What cities in Texas are hiring for Quality Control Biotechnology jobs? Cities in Texas with the most Quality Control Biotechnology job openings:
Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $40,631 per year, or $19.5 per hour.

Quality Control Manager

Resilience Texas LLC

Houston, TX • On-site

Full-time

Posted 2 days ago

New

Job description

POSITION TITLE: QC Manager


Location: Houston, TX Onsite
Department: Quality Control
Reports to: Associate Director, Quality Control

About CTMC

CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, and located in the renowned Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, ETC, and TCR-T. Our expert team collaborates closely with MD Anderson’s research and clinical faculty, bringing impactful cell therapies to cancer patients.


In our first year alone, we have filed four INDs, each ahead of schedule, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience, an ambitious biomanufacturing organization that has raised $2 billion in two years, enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results.


Our state-of-the-art, 60,000 sq. ft. facility in the Texas Medical Center is staffed by an integrated team of over 80 industry veterans and scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our mission.

At CTMC, we value our employees and offer a variety of development opportunities within our organization. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission.

Key Responsibilities:

The QC Manager will provide technical and operational oversight for analytical testing activities supporting clinical and pivotal-stage Cell and Gene Therapy (CGT) programs transitioning toward commercial readiness. This role will lead testing execution, ensure compliance with GMP requirements, and support method qualification and validation activities for advanced analytical platforms including flow cytometry, molecular assays, and ELISA.

The ideal candidate is a strong technical leader with demonstrated expertise in flow cytometry data analysis, molecular testing methodologies, and ELISA platforms within CGT manufacturing environments.

  • Provide day-to-day supervision of QC analytical staff performance:
  • Flow cytometry analysis (multicolor panels, CAR detection, phenotyping, functional assays).
  • Molecular assays (e.g., qPCR/ddPCR, vector copy number, gene expression)
  • ELISA-based potency and cytokine assays
  • Ensure testing activities support clinical Phase I/II, pivotal, and commercial readiness programs.
  • Oversee data review, trending, and technical evaluation to ensure data integrity and compliance with 21 CFR Part 211 and Part 11 requirements.
  • Lead or support analytical method qualification and validation activities per ICH guidelines
  • Support transfer of analytical methods from Development to QC.
  • Participate in investigations, deviations, OOS/OOT events, and CAPAs related to analytical testing.
  • Ensure proper documentation practices and adherence to internal SOPs and regulatory standards.
  • Support regulatory inspections and client audits as SME for analytical platforms.
  • Contribute to readiness for commercial-scale manufacturing and lifecycle management.
  • Perform daily lab tasks and support adherence to production and testing schedules.
  • Assist in the execution of method, equipment, and process validation/qualification activities in accordance with ICH guidelines, cGMP, cGTP, and other applicable regulatory standards.
  • Support reference standard characterization and data trending.
  • Ensure lab readiness for internal and external audits by maintaining compliance with regulatory and quality standards.
  • Assist with inventory management to support uninterrupted laboratory operations.
  • Maintain general laboratory organization, cleanliness, and compliance with 5S principles.
  • Perform other duties as assigned to support department and company goals.

Qualifications/Skills

  • Bachelor’s degree in science field required or equivalent combination of education and experience.
  • 7+ years of experience in GMP QC laboratory within Cell and Gene Therapy or biologics manufacturing.
  • Advanced experience in:
    • Flow cytometry analysis (panel design, gating strategy, data interpretation)
    • Molecular analytical methods (qPCR/ddPCR preferred)
    • ELISA assay execution and data interpretation
  • Demonstrated experience supporting pivotal-stage or commercial readiness programs.
  • Direct experience in analytical method qualification and/or validation under GMP.
  • Strong understanding of data integrity, electronic systems, and regulatory expectations.
  • Experience supervising or mentoring technical staff preferred.
  • Capable of working in a fast-paced environment and communicating effectively with a diverse work group.

Preferred Experience

  • Experience supporting regulatory inspections (FDA, EMA).
  • Experience with CAR-T or gene-modified cell therapy products.
  • Familiarity with analytical lifecycle management and assay robustness improvement.
  • Experience with LIMS or electronic data systems.

Core Competencies

  • Strong technical troubleshooting skills
  • Ability to interpret complex analytical datasets
  • Leadership and team development
  • Regulatory and compliance mindset
  • Cross-functional collaboration (QA, AD, Manufacturing)

Working Conditions, Equipment, Physical Demands

The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands:

Equipment-

  • Computer
  • Printer
  • Scanner
  • Telephone
  • Lab Equipment


Physical Demands-

  • Frequent sitting, standing, walking
  • Carrying packages and moving bins and boxes, lifting up to 10 lbs.

The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act.

The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.