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Quality Control Biotechnology Jobs in Texas (NOW HIRING)

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 ...

NTG Staffing

EM Tech II

The Woodlands, TX · On-site

$28/hr

Works in a fast-paced environment supporting the quality control department of a CMDO for ... the biotech, pharmaceutical, or cell/gene therapy industries. Have the knowledge and ability to ...

NTG Staffing

EM Tech II

The Woodlands, TX · On-site

$28/hr

Works in a fast-paced environment supporting the quality control department of a CMDO for ... biotech, pharmaceutical, or cell/gene therapy industries. • Have the knowledge and ability to ...

Charles River Laboratories, Inc.

... change control, and internal audit activities. • Communicate all identified quality and ... Our client base includes global pharmaceutical companies, biotechnology companies, government ...

Lonza

Quality Assurance Specialist IV

Houston, TX · On-site

The position partners closely with Manufacturing, Quality Control, and Quality Systems teams to ... Biotechnology, Life Sciences, Engineering, or a related scientific discipline is required. • ...

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How much do quality control biotechnology jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for quality control biotechnology in Texas is $19.53, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $21.49 per hour, depending on experience, location, and employer.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

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

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

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

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

How to become a quality control biotechnology specialist?

To become a quality control biotechnology specialist, candidates typically need a bachelor's degree in biotechnology, biology, or a related field. Gaining experience with laboratory techniques, quality assurance protocols, and regulatory standards such as GMP or ISO is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail, analytical skills, and familiarity with laboratory equipment are also essential for success in this role.

What does quality control biotechnology do in biotech?

Quality Control Biotechnology professionals are responsible for testing and analyzing biological products to ensure they meet safety, quality, and regulatory standards. They perform assays, validate processes, and document results using laboratory instruments and techniques, often working under Good Manufacturing Practice (GMP) guidelines. Their work helps ensure the integrity and compliance of biotech products before they reach the market.

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

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

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

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

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

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

Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology 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, with an average salary of $40,631 per year, or $19.5 per hour.

Quality Control Chemist II

Radiomedix, Inc.

Humble, TX • On-site

Full-time

Re-posted yesterday

Job description

Mission:
Ensures quality control efforts are performed in accordance with established chemistry, manufacturing, and controls specifications for Ga68 generators and upcoming projects in the pipeline.
Quality Control Responsibilities:
  • 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 for the patient/end user
  • Follows pertinent RadioMedix Quality Control procedures for e.g. Identity testing, radiochemical purity, radionuclidic purity, endotoxin and sterility
  • Preforms analytical testing with proficiency in equipment e.g. HPLC, TLC, ICPMS, HPGE/Gamma Spec
  • Completes and maintains appropriate documentation required by federal and state agencies
  • Sets up and maintains automated chemistry modules and laboratory equipment
  • Supports RadioMedix's development of radiochemical processes
  • Ensures Quality Control methods are in conformity with cGMP
  • Assist in the development of procedures, test reports, operating procedures, and maintenance procedures for new or updated processing equipment.
  • Drafts pertinent protocols, reports and documentation to support API and Drug Product
  • Tests materials upon incoming receipt if required according to RadioMedix release specifications
  • Ensures chemicals on site are properly managed in appropriate conditions with appropriate documentation e.g. Safety Data Sheets
  • Trains new QC employees
  • Coordinates third party testing of raw materials if required
Analytical Method Development Responsibilities:
  • Development of procedures in the quality control of radiopharmaceuticals/API using a variety of instruments such as HPLC, GC, TLC, and ICP-MS.
  • Develop and improve analytical methods used in assessing the radiochemical attributes of the company products
  • Write necessary SOPs, Validation Protocols and Validation Report
Radiation Safety responsibilities:
  • Supports wipes and surveys of the facility to ensure state of control
  • Provides basic support and supervision for ensuring calibration of all radiation instrumentation
  • Performs radiation safety duties to assure compliance with all regulations.
  • Assesses the nuclear waste characteristics of the group's chemical processes to support regulatory and waste classification exercises.
Other Responsibilities:
  • Be self-motivated and able to work as a team member when needed
  • Ensures a safe and quality working environment through training, awareness, and compliance to safety guidelines and SOP's.
  • Follows and promote on-the-job safety expectations, including wearing proper Personal Protective Equipment (PPE) and following cGMP rules and guidelines in all designated areas.
  • Ability to meet the physical demands of the job (standing for long periods of time, lifting heavy loads of up to 40 pounds etc.)

Work Environment:
Location: RadioMedix Spica Center, 19705 Aldine Westfield Rd, Humble, TX
Work Conditions:
The work environment consists of manufacturing, laboratory and office spaces. The position will sometimes require more than forty hours of work per week. The work period is typically between 8:30 AM to 5 PM.
Individuals in this position will be exposed to ionizing radiation; however, radiation safety training will be provided and radiation monitoring is required and ongoing at the facilities. Any exposure will be within Federal and State limits. Individuals in this position are required to be able to function and maneuver within the work environment without placing self, the product or others at risk.
The position requires physical strength and dexterity with the ability to climb on ladders and up on equipment for environmental service and maintenance responsibilities.

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