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Weekend Biotech Quality Control Jobs in Houston, TX

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 ...

OmniForce

Quality Control Inspector

Houston, TX · On-site

... or weekends as needed Quality Control Inspector Preferred: Certificate in quality control, electrical technology, or related field Certified Quality Inspector (CQI) certification OSHA 10 ...

Onin Staffing

Quality Control Tester

Brookshire, TX

$22/hr

Plus, radically affordable health insurance after 30 days. - 1st Shift, Flex/Flexible, Weekend ... Quality Control Tester - Perform quality control testing - Troubleshoot basic test failures ...

Amrize

Quality Control Apprentice

Humble, TX · On-site

$15.75 - $20/hr

Willingness to work nights and weekends. * Teamwork with QC, operations and drivers. * Self motivated. * Positive communication with customers and labs during issues. * Education: High school diploma ...

Gulf Coast Blood

Quality & Control Technician

Houston, TX · On-site

$18 - $23/hr

Quality & Control Technician I Join our team of heroes! Are you seeking daily adventure while ... Weekend and Holidays - Must be available and willing to work such weekends and holidays as are ...

National Strand Products, LP

QC Technician

Baytown, TX · On-site

$16.75 - $21.50/hr

Rotating shifts, overtime and weekend work may be required as job duties demand. Travel - This ... by the QC Technician position to successfully perform the essential functions of this job.

ALTIVIA

QC Lab Technician

Crosby, TX

$20 - $25.25/hr

Crosby, Texas - Must be able to work rotating shifts, including weekends and holidays. Job Summary The QC Lab Technician is responsible for testing raw materials, in-process samples, and finished ...

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How much do weekend biotech quality control jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for weekend biotech quality control in Houston, TX is $20.51, according to ZipRecruiter salary data. Most workers in this role earn between $16.54 and $22.93 per hour, depending on experience, location, and employer.

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Weekend Biotech Quality Control jobs near you
Infographic showing various Weekend Biotech Quality Control job openings in Houston, TX as of August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 100% In-person job distribution, with an average salary of $42,657 per year, or $20.5 per hour.

Quality Control Manager

Resilience Texas LLC

Houston, TX • On-site

Full-time

This job post has expired today. 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.