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Quality Control Laboratory Manager Jobs in Texas

POSITION TITLE: QC Manager Location : Houston, TX Onsite Department: Quality Control Reports to ... Maintain general laboratory organization, cleanliness, and compliance with 5S principles. * Perform ...

QC Lab Technician

Crosby, TX

$20 - $25.25/hr

This position provides technical support to plant operations and internal teams through laboratory analysis, data management, equipment maintenance, and quality assurance activities. The QC Lab ...

QC Lab Technician

Mckinney, TX ยท On-site

$19 - $22/hr

QC Laboratory Technician The QC Lab Technician is responsible for performing routine laboratory ... of laboratory equipment, reporting any malfunctions to management. o Ensure that equipment is ...

QC Lab Manager

Carrollton, TX ยท On-site

$90 - $120/hr

The Role The Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

New

$100 - $140/hr

The Role The Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

New

Quality Control Manager

Lubbock, TX ยท On-site

$130K - $165K/yr

Direct laboratory operations, quality systems, and accreditation requirements. * Ensure compliance ... Develop, mentor, and lead regional quality control managers, laboratory managers, technicians, and ...

The RoleThe Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

The Role The Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

The Role The Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

The Role The Quality Control Lab Manager will manage and direct the day-to-day operation of the QC laboratory. This individual will be responsible for providing leadership to the laboratory resources ...

Sr. Scientist, Quality Control

Plano, TX ยท On-site

$160K - $175K/yr

Sr. Scientist, Quality Control Department: 64 - Quality Control Employment Type: Full Time Location ... Manage the lifecycle of analytical methods and laboratory instruments, including qualification ...

Quality Laboratory Technician

El Paso, TX ยท On-site

$15.50 - $19.75/hr

As a Quality Laboratory Technician, you will be responsible for performing chemical and physical ... Control and management ofretained/rejected material. Documentation & Reporting * Review and verify ...

Quality Laboratory Technician

El Paso, TX ยท On-site

$15.50 - $19.75/hr

As a Quality Laboratory Technician, you will be responsible for performing chemical and physical ... Control and management of retained/rejected material. Documentation & Reporting * Review and verify ...

Quality Laboratory Technician

El Paso, TX ยท On-site

$15.50 - $19.75/hr

As a Quality Laboratory Technician, you will be responsible for performing chemical and physical ... Control and management of retained/rejected material. Documentation & Reporting * Review and verify ...

Showing results 21-40

Quality Control Laboratory Manager information

What does a quality control laboratory manager do?

A Quality Control Laboratory Manager oversees the operations of a laboratory that tests products for quality and compliance with industry standards. They manage laboratory staff, ensure testing procedures are followed accurately, and maintain equipment. The manager is responsible for implementing quality assurance protocols, analyzing test results, and reporting findings to upper management. Their work helps ensure that products meet safety and quality requirements before reaching consumers.

What are the key skills and qualifications needed to thrive as a quality control laboratory manager?

To thrive as a Quality Control Laboratory Manager, you need a strong background in laboratory science, quality assurance, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and certifications such as ASQ Certified Quality Auditor are often required. Excellent leadership, problem-solving, and communication skills help manage teams and ensure smooth operations. These competencies are crucial for maintaining high standards, ensuring product safety, and meeting regulatory requirements in laboratory environments.

What are some common challenges faced by quality control laboratory managers, and how can they be addressed?

Quality Control Laboratory Managers often face challenges such as maintaining compliance with strict regulatory standards, managing a diverse team, and ensuring timely turnaround of test results. To address these, effective managers implement robust training programs, foster clear communication across teams, and establish standardized operating procedures. Proactive planning and continuous process improvement are key to staying ahead of regulatory updates and ensuring consistent data quality, which ultimately supports both operational efficiency and product safety.

What is the difference between Quality Control Laboratory Manager vs Quality Control Analyst?

AspectQuality Control Laboratory ManagerQuality Control Analyst
CredentialsBachelor's degree in science, often with management certificationsBachelor's degree in science or related field
Work EnvironmentSupervises lab staff, manages operations, oversees testing processesPerforms testing and analysis of samples under supervision
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for lab oversightCommonly employed in similar industries for sample analysis

The main difference is that the Quality Control Laboratory Manager oversees the entire lab operations and staff, ensuring compliance and quality standards, while the Quality Control Analyst focuses on conducting specific tests and analyses. The manager has more responsibilities related to supervision and process management, whereas the analyst is primarily involved in testing tasks.

What are the most commonly searched types of Quality Control Laboratory jobs in Texas?

The most popular types of Quality Control Laboratory jobs in Texas are:

What cities in Texas are hiring for Quality Control Laboratory Manager jobs?

Cities in Texas with the most Quality Control Laboratory Manager job openings:

Infographic showing various Quality Control Laboratory Manager job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Quality Control Manager

Resilience Texas LLC

Houston, TX โ€ข On-site

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


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.