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Overnight Biotech Quality Control Jobs in Spring, 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

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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 ...

Connect Staffing

Quality Control Inspector

Houston, TX · On-site

$18 - $21/hr

Connect Staffing is hiring a Quality Control Technician for an oilfield drilling components ... This position runs a consistent Monday-Friday overnight schedule with steady work and long-term ...

Connect Staffing

Quality Control Inspector

Houston, TX · On-site

$18 - $21/hr

Connect Staffing is hiring a Quality Control Technician for an oilfield drilling components ... This position runs a consistent Monday-Friday overnight schedule with steady work and long-term ...

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Overnight Biotech Quality Control information

See Spring, TX salary details

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

As of Aug 7, 2026, the average hourly pay for overnight biotech quality control in Spring, TX is $18.66, according to ZipRecruiter salary data. Most workers in this role earn between $16.06 and $20.53 per hour, depending on experience, location, and employer.

What is the difference between Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

What are some common challenges faced by overnight biotech quality control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What is an overnight biotech quality control?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What are the key skills and qualifications needed to thrive as an overnight biotech quality control professional?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.
What are popular job titles related to Overnight Biotech Quality Control jobs in Spring, TX? For Overnight Biotech Quality Control jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Overnight Biotech Quality Control jobs in Spring, TX look for? The top searched job categories for Overnight Biotech Quality Control jobs in Spring, TX are:
What cities near Spring, TX are hiring for Overnight Biotech Quality Control jobs? Cities near Spring, TX with the most Overnight Biotech Quality Control job openings:
Overnight Biotech Quality Control jobs near you

Quality Control Manager

Resilience Texas LLC

Houston, TX • On-site

Full-time

Posted 3 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.