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Quality Control Analyst Per Diem Jobs in Spring, TX

Kellton Tech

QC Micro EM Analyst II

Houston, TX · On-site

$25 - $33/hr

Quality Control Environmental Monitoring Technician Location: Houston, TX (Onsite) Pay Range: $25 ... Contribute to revising SOPs, deviation reports, trend analyses, and corrective actions * Execute ...

Control Devices LLC

QC Inspector

Houston, TX · On-site

Conducts routine and non-routine analysis of raw materials, in-process, and finished product, using ... Proficient in Calibration data entry and protocol per standardsPhysical RequirementsThe physical ...

Control Devices, LLC

QC Inspector

Houston, TX

Conducts routine and non-routine analysis of raw materials, in-process, and finished product, using ... Proficient in Calibration data entry and protocol per standards Physical Requirements The physical ...

Control Devices LLC

QC Inspector

Houston, TX · On-site

Conducts routine and non-routine analysis of raw materials, in-process, and finished product, using ... Proficient in Calibration data entry and protocol per standards Physical Requirements The physical ...

Umicore

QC Analytical Laboratory Manager

Pasadena, TX · On-site

Job Summary We are seeking a QC Analytical Laboratory Manager to provide technical, operational and people leadership for our quality-control analytical laboratory supporting stationary catalyst ...

Seatrium

Quality Control Engineer

Houston, TX

The Quality Control Engineer is responsible for ensuring that all materials, equipment, and ... Strong analytical skills to assess quality issues, analyze data, and implement corrective actions.

Apache Workforce LLC

Quality Control Manager

Houston, TX · On-site

$95K - $115K/yr

Quality Control Manager Apache Fabricators - Houston, TX Pay: $95,000 - $115,000 per year DOE Schedule: Monday - Saturday | First Shift FABRICATION SHOP EXPERIENCE REQUIRED Apache Fabricators is ...

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All JobsQuality Control Analyst Per Diem JobsQuality Control Analyst Per Diem Jobs in Spring, TX

Quality Control Analyst Per Diem information

See Spring, TX salary details

$14

$24

$36

How much do quality control analyst per diem jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for quality control analyst per diem in Spring, TX is $24.84, according to ZipRecruiter salary data. Most workers in this role earn between $20.53 and $27.60 per hour, depending on experience, location, and employer.

What is a quality control analyst per diem?

Quality Control Analyst Per Diem jobs are positions where professionals are responsible for testing and ensuring the quality of products, typically in industries like pharmaceuticals, food, or manufacturing, but work on an as-needed or temporary basis. 'Per diem' means 'per day,' so these analysts are usually hired to fill in for regular staff, handle increased workloads, or assist with special projects. Their primary duties include sampling, testing materials, documenting results, and ensuring compliance with regulatory standards. Per diem roles offer flexibility but may not guarantee regular hours or benefits.

What does a quality control analyst per diem do?

As a Quality Control Analyst Per Diem, you are responsible for performing laboratory tests on raw materials, in-process samples, and finished products to ensure compliance with regulatory and company standards. Your work typically includes documenting results, identifying deviations, and communicating findings to production and quality assurance teams. Since this is a per diem position, you may be called upon to support peak workloads or cover for absent staff, requiring flexibility and adaptability. Your contributions are crucial in maintaining product integrity, minimizing recalls, and ensuring customer safety. Collaboration with other departments, such as manufacturing and R&D, is common to address and resolve quality issues efficiently.

What skills and qualifications are needed to thrive as a quality control analyst per diem?

To thrive as a Quality Control Analyst Per Diem, you need a solid understanding of laboratory testing, analytical techniques, and quality assurance principles, generally supported by a bachelor's degree in a scientific field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or GC is typically required. Strong attention to detail, problem-solving skills, and effective communication are essential soft skills in this role. These competencies ensure that products meet strict quality standards and regulatory requirements, which is vital for consumer safety and organizational compliance.

What is the difference between Quality Control Analyst Per Diem vs Quality Control Analyst?

AspectQuality Control Analyst Per DiemQuality Control Analyst
Work ScheduleTemporary, on-call, or daily assignmentsFull-time, permanent position
CertificationsTypically requires industry certifications (e.g., GMP, GLP)Same certifications as Per Diem role
Work EnvironmentLaboratory or manufacturing settings, often in multiple locationsConsistent workplace, often in a single facility
Employment TypePer diem, often with flexible hoursFull-time employment with benefits

Both roles require similar credentials and work in laboratory or manufacturing environments. The key difference is that Per Diem positions are temporary and flexible, while full-time roles offer stability and benefits.

What are the most commonly searched types of Quality Control Analyst jobs in Spring, TX?

The most popular types of Quality Control Analyst jobs in Spring, TX are:

What cities near Spring, TX are hiring for Quality Control Analyst Per Diem jobs?

Cities near Spring, TX with the most Quality Control Analyst Per Diem job openings:

Quality Control Analyst Per Diem jobs near you
Infographic showing various Quality Control Analyst Per Diem job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $51,672 per year, or $24.8 per hour.

Quality Control Manager

Resilience Texas LLC

Houston, TX • On-site

Full-time

Posted 13 days ago

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.