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Quality Control Pharma Jobs in Texas (NOW HIRING)

Quality Control Laboratory Specialist

Coppell, TX · On-site

$18.25 - $23.25/hr

Quality Control Team Member Location: Coppell TX Shift: Monday through Friday, 6 am to 3 pm ... in a pharma industry lab without a degree Most important things to be considered: * 2 years of ...

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 ...

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 ...

QC CHEMIST II

Rosenberg, TX · On-site

$25 - $32/hr

  • Medical

  • Dental

  • Vision

  • Retirement

At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates ...

Quality Control Chemist II

Rosenberg, TX

$25 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Quality Control Chemist II Kelly ® Science & Clinical is seeking a Quality Control Chemist II for a premier pharma company in Rosenberg, TX . If you're passionate about bringing the latest ...

SENIOR QC CHEMIST

Rosenberg, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

Collaborate with cross-functional teams, including Quality Assurance, Production, and R&D. * Assist ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

Provide Quality Control laboratory service to fulfill pharmaceutical requirements pertaining to finished products manufactured by or for Kavis Pharma LLC. Assure quality of products through testing ...

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Lab Tech I

Waco, TX · On-site

CA$18 - CA$19/hr

Perform routine analytical testing to support quality control testing of pharmaceutical products. Some data interpretation required. have good laboratory skills, preferably in pharma/biotech.

Thorough knowledge of cGMPs, GLPs, and pharma manufacturing * Ability to collaborate with cross-functional teams including research, process development, quality assurance and quality control.

Quality Assurance Specialist

Houston, TX · On-site

$32 - $35/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Provide timely and high-quality data to support Quality Control Unit (QCU) disposition decisions ... Pharma manufacturing experience * Preferred: Strong Microsoft Excel experience Skills * Technical ...

Thorough knowledge of cGMPs, GLPs, and pharma manufacturing * Ability to collaborate with cross-functional teams including research, process development, quality assurance and quality control.

QA Specialist III (Sunday-Thursday,11p-8a)

Houston, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material ... GMP experience in the biologics and pharma industry. * Working knowledge of equipment/facilities ...

QA Specialist III (Sunday-Thursday,11p-8a)

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material ... GMP experience in the biologics and pharma industry. * Working knowledge of equipment/facilities ...

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Showing results 1-20

Quality Control Pharma information

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

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

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

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

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Texas?

For Quality Control Pharma jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Texas look for?

The top searched job categories for Quality Control Pharma jobs in Texas are:

What cities in Texas are hiring for Quality Control Pharma jobs?

Cities in Texas with the most Quality Control Pharma job openings:

Infographic showing various Quality Control Pharma 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 Technician (Wilcrest Pharma)

Wilcrest Pharma

Houston, TX • On-site

$19.75 - $25.50/hr

Full-time

Re-posted 12 days ago


Job description

What We Are Looking For
As a Quality Control Technician, you will play an important role in helping Wilcrest Pharma deliver safe, high-quality sterile and non-sterile medications. In this role, you will support QC testing activities, sample management, environmental monitoring, finished product inspection, labeling, and packaging support.
What You Will Do
• Collect, prepare, and coordinate samples for third-party testing, ensuring proper chain of custody documentation, storage and timely submission.
• Conduct environmental monitoring (EM) activities including viable air, surface, and personnel monitoring within manufacturing areas.
• Execute assigned qualification and validation activities, including environmental monitoring studies, equipment qualification activities, and sample collection.
• Maintain QC sample inventory, including retention samples, stability samples, and in-process controls, ensuring proper storage and documentation.
• Perform assigned finished product inspection and packaging support activities, including visual inspection, product labeling, label verification/reconciliation, heat sealing, and completion of required documentation.
• Review laboratory and third-party testing data for accuracy, completeness, and compliance with approved specifications.
• Support quality investigations related to out-of-specification (OOS) results, environmental monitoring excursions, inspection discrepancies, labeling issues, and packaging concerns.
• Coordinate with third-party laboratories to schedule routine, release, and stability testing and support timely reporting and documentation of results.
• Support preparation for regulatory inspections, customer audits, and internal audits by helping maintain accurate, complete, and inspection-ready QC documentation.
• Maintain and upload QC records into the electronic documentation management system to support traceability and CGMP compliance.
• Collaborate with Production and other cross-functional teams as needed, and perform additional duties as assigned by the Director of Quality.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.