ZipRecruiter

Log In

1

Quality Control Stability Jobs in Texas (NOW HIRING)

US Modules

Quality Control Operator

College Station, TX · On-site

$14 - $17.25/hr

Position Summary The Quality Control Operator is responsible for inspecting and electrically ... and system stability monitoring * Ensure calibration status, reference devices, and test ...

Triple-S Steel

Quality Control Tech

Houston, TX · On-site

$18 - $23/hr

Stability: All decisions made are measured in years, not quarters. Flexibility: Employees are ... industry/quality control Knowledge/Skills/Competencies: * General Product Knowledge

Triple-S Steel

Quality Control Tech

Houston, TX · On-site

$18 - $23/hr

Stability: All decisions made are measured in years, not quarters. Flexibility: Employees are ... industry/quality control Knowledge/Skills/Competencies: * General Product Knowledge

Codexis Inc

Sr. Scientist, Quality Control

Plano, TX · On-site

$160K - $175K/yr

Design, execute, and oversee stability programs, including protocol development, study execution, data review, trend evaluation, and technical reporting. * Support QC systems, documentation ...

Cellipont Bioservices

QC Lead Analyst

The Woodlands, TX

$21.50 - $28.75/hr

The QC Lead Analyst works in a fast-paced environment supporting the quality control department of ... stability samples. * Author, review, and/or approve SOPs, test methods, material specifications ...

Cellipont Bioservices

QC Lead Analyst

Spring, TX · On-site

$22 - $29.50/hr

The QC Lead Analyst works in a fast-paced environment supporting the quality control department of ... stability samples. * Author, review, and/or approve SOPs, test methods, material specifications ...

Cellipont Bioservices

QC Lead Analyst

The Woodlands, TX · On-site

$22 - $29.50/hr

The QC Lead Analyst works in a fast-paced environment supporting the quality control department of ... stability samples. * Author, review, and/or approve SOPs, test methods, material specifications ...

Sovereign Pharmaceuticals

QC Lab Technician

Fort Worth, TX · On-site

$19 - $24/hr

... Stability Program management (sample placement/retrieval from the chambers) • Assist with retaining sample storage/retrieval ESSENTIAL FUNCTIONS • Supporting QC Laboratory operations by ...

DebtBlue

Payment Processor (QC Team)

Richardson, TX · On-site

Quality Control Specialist - Quality Control Department DebtBlue, LLC is a fastgrowing debt settlement organization committed to helping individuals and families regain financial stability. We serve ...

DebtBlue

Payment Processor (QC Team)

Richardson, TX · On-site

$18/hr

Quality Control Specialist - Quality Control Department DebtBlue, LLC is a fast-growing debt settlement organization committed to helping individuals and families regain financial stability. We serve ...

DebtBlue

Payment Processor (QC Team)

Richardson, TX · On-site

$18/hr

Quality Control Specialist - Quality Control Department DebtBlue, LLC is a fast‑growing debt settlement organization committed to helping individuals and families regain financial stability. We ...

CYNET SYSTEMS

Spec 1, Quality Control

El Paso, TX · On-site

$21 - $26/hr

... finished products, and stability samples according to applicable procedures. * Collects ... and/or Quality Manager/Designee in order to achieve QC testing delivery goals. * Maintains ...

CYNET SYSTEMS

Quality Control Specialist I

El Paso, TX · On-site

$21 - $26/hr

... finished products, and stability samples according to applicable procedures. * Collects ... QC testing delivery goals. * Maintains Microbiology Lab audit readiness. Qualification And ...

next page

Showing results 1-20

All JobsQuality Control Stability JobsQuality Control Stability Jobs in Texas

Quality Control Stability information

What career paths are possible in QC?

Career paths in Quality Control (QC) include roles such as QC Technician, QC Analyst, Quality Assurance Specialist, and Quality Manager. Advancement often involves gaining experience, certifications like ASQ certifications, and developing skills in inspection, testing, and data analysis within manufacturing, pharmaceuticals, or food industries.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Which pays more, QA or QC?

In the field of Quality Control Stability, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities and focus on process improvement. QA jobs often require more experience and may involve certifications like Six Sigma or ISO standards, which can also influence pay. However, salaries vary based on industry, location, and level of experience.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

Is QC analyst a stressful job?

A QC analyst role involves inspecting and testing products to ensure quality standards are met, which can be demanding during tight deadlines or when addressing product issues. The job often requires attention to detail, adherence to safety protocols, and sometimes working in environments with strict regulatory requirements, which can contribute to stress levels.

What is quality control salary?

The salary for a quality control stability role typically ranges from $40,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher wages. Salaries often include benefits such as health insurance and paid time off.
What are the most commonly searched types of Quality Control Stability jobs in Texas? The most popular types of Quality Control Stability jobs in Texas are:
What are popular job titles related to Quality Control Stability jobs in Texas? For Quality Control Stability jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Texas look for? The top searched job categories for Quality Control Stability jobs in Texas are:
What cities in Texas are hiring for Quality Control Stability jobs? Cities in Texas with the most Quality Control Stability job openings:
Quality Control Stability jobs near you

Quality Control Scientist III

Velocity Bioworks

San Antonio, TX • On-site

Full-time

Re-posted 14 days ago

Job description

TITLE: Quality Control Scientist III
REPORTS TO: Manager, Quality Control
LOCATION: San Antonio, Texas (Onsite)
Note: This position has a July 2026 start date.
The Company
Velocity Bioworks is a U.S.-based biopharma CDMO headquartered in San Antonio, Texas supporting funded programs as they move from development into manufacturing for clinical trials. We collaborate with sponsors who are past exploration and are ready to apply discipline, structure, and technical rigor to development, analytics, and manufacturing.
Velocity is built to accelerate speed to clinic through aligned execution. Our work focuses on translating defined program goals into scalable manufacturing processes and robust analytical strategies. These activities are designed to support near-term clinical timelines while meeting quality requirements. We operate where quality and execution directly influence clinical and business progress.
Position Summary
Reporting directly to the Manager, Quality Control, the Quality Control Scientist III, demonstrates full understanding of scientific and technical aspects of biological Drug Product/Drug Substance (DP/DS), as well as technology transfer, assay qualifications and validations activities. The Quality Control Scientist III is responsible for performing routine, In-process, and stability testing of drug products and analysis of raw materials, intermediates, and finished products, utilizing various analytical techniques and methods. This job might be for you if you enjoy working in a fast-paced environment and you have the skills to balance multiple tasks, prioritize them, and complete them independently while excelling at keeping all impacted parties well-advised. An ideal candidate must have strict attention to detail, high-quality customer service skills, and the ability to work well and collaborate in cross-functional teams at Velocity Bioworks .
Key Responsibilities
  • Conduct assays and lab procedures according to and in compliance with CGMP guidelines and internal SOPs.
  • Performing routine, In-process and stability testing analysis of raw materials, intermediates, and finished products, utilizing various analytical techniques and methods.
  • Ensure testing is completed in compliance with all applicable procedures, standards, and CGMP regulations.
  • Work with Analytical Development team, Quality and Operations organization to successfully transfer process/analytical testing to the CGMP facility to manufacture products.
  • Ensure all analytical data from the laboratory is accurate, precise, robust and is generated following methods, specifications, and procedures.
  • Ensure compliance with training, testing, documentation, and general lab maintenance requirements for industry standards and/or regulations.
  • Perform tasks in a manner consistent with the safety policies, quality systems and CGMP requirements.
  • Investigate Out-of-Specification (OOS) results and laboratory deviations, conduct root cause analysis, and implement CAPA.
  • Ensure successful method transfer, including training of personnel for execution and review, review of data, and completion of documentation.
  • Responsible for ensuring all QC laboratory equipment is maintained and calibrated according to schedule.
  • Shifts may include routine weekend and evening work as required by the manufacturing process.
  • Train junior staff on new methods of tech transfers.

Knowledge & Skills
  • Candidate should be familiar with analytical and QC operations in the pharmaceutical industry and understand key regulations and trends in biologics development and manufacturing, including CGMP, FDA, ICH, USP, EMA, and global compendia guidance.
  • Working experience in quality control operation to support clinical and commercial scale manufacturing, product testing, and regulatory IND/BLA filing.
  • Strong technical and scientific knowledge of general QC testing.
  • Hands-on experience in modern analytical instruments and methods, such as HPLC, UPLC, CE, iCE, ELISA, qPCR, pH, Appearance, Osmolality, Total Organic Content, Endotoxin, Western Blotting, LC-MS/MS and Cell-based Bioassays.
  • Ability to evaluate technical data
  • Provides training on areas of technical expertise and compliance issues relevant to the lab setting.
  • Working experience with performing industry investigations/deviations.
  • Working experience with analytical method qualification and validations.
  • Working experience with training analysts on new transfer methods.
  • Experience with lab-based software systems such as: LIMS/ELN, Empower, including validation of templates within these systems.
  • Excellent communication skills with the ability to collaborate across multiple teams and projects.
  • Experience with speaking publicly. Able to maintain control of meetings as required.

Requirements
Education & Experience
  • Bachelor or advanced Graduate degree (MS/PhD) in Chemistry, Biological Sciences Microbiology, Biochemistry or equivalent field.
  • 4+ years of relevant experience or equivalent for Bachelors' or 3+ years of relevant experience or equivalent for Masters or PhD with 1+ year in QC operations

Physical Requirements & Working Environment
  • Flexibility is required for working hours. Some weekend work may be needed and earlier or later start/finish times may also be required.
  • The essential functions of the job are usually performed in an environmentally controlled facility where the noise level in the work environment is usually moderate. This position may involve a combination of office and laboratory environments and automated equipment.
  • While performing the job duties, the employee is regularly required to sit; reach with hands and arms and talk or hear. The employee is frequently required to stand and walk. The employee may sometimes be required to lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision and ability to adjust focus. The employee must have the manual dexterity and manual ability to effectively use computer terminals.

Notice to Third Party Agencies: Velocity Bioworks does not accept unsolicited resumes from recruiters or employment agencies. In the event a recruiter or agency submits a resume or candidate without a previously assigned agreement and approved engagement request with Velocity Bioworks, Velocity Bioworks reserves the right to pursue and hire the candidate(s) without any financial obligation to the recruiter or agency.
Velocity Bioworks is proud to be an EEO/AAP Employer. Velocity Bioworks encourages protected veterans, individuals with disabilities, and applicants from all backgrounds to apply. Velocity Bioworks ensures nondiscrimination in all programs and activities in accordance with Title VI of the Civil Rights Act.

Apply