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Senior Quality Control Analyst Jobs in Texas (NOW HIRING)

MVT Holdings

Quality Control Analyst

El Paso, TX · On-site

$45K - $55K/yr

Join our family at MVT Warehousing (Stagecoach)! We're seeking a Quality Control Analyst in El Paso, TX! Job Summary The Quality Control Analyst is responsible for monitoring, auditing, and analyzing ...

Astrix Inc

Quality Control Analyst II

Fort Worth, TX · On-site

$23 - $31/hr

  • Medical

  • Dental

  • Retirement

  • PTO

Pay Rate Low: 28.00 | Pay Rate High: 32.00 Exciting Quality Control Analyst II development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device ...

Tindall Corporation

QC Analyst

San Antonio, TX · On-site

$21.75 - $29/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Data Analysis & Reporting * Collects, analyzes, and interprets QC data to identify trends and improvement opportunities. * Prepares weekly and monthly quality performance reports for management.

Tindall

QC Analyst

San Antonio, TX · On-site

$21.75 - $29/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Data Analysis & Reporting * Collects, analyzes, and interprets QC data to identify trends and improvement opportunities. * Prepares weekly and monthly quality performance reports for management.

New

Providencia

Quality Control Analyst

El Paso, TX

$21.75 - $29.25/hr

Quality Control Analyst LOCATION: Onsite: El Paso, TX About Us The Providencia Group is led by a purpose: to address global challenges and make an impact that matters through delivering ...

The Providencia Group

Quality Control Analyst

El Paso, TX · On-site

$21.75 - $29.25/hr

Quality Control Analyst LOCATION: Onsite: El Paso, TX About Us The Providencia Group is led by a purpose: to address global challenges and make an impact that matters through delivering ...

Stellantis Financial Services

QC Analyst

Houston, TX · On-site

$22 - $29.50/hr

The QC Analyst will be responsible for performing audits of the various functional areas within the organization, including but not limited to: State Changes, Releases, Collateral Management ...

Stellantis Financial Services

QC Analyst

Houston, TX · On-site

$23 - $30.75/hr

The QC Analyst will be responsible for performing audits of the various functional areas within the organization, including but not limited to: State Changes, Releases, Collateral Management ...

Stellantis Financial Services US

QC Analyst

Houston, TX

$22 - $29.50/hr

The QC Analyst will be responsible for performing audits of the various functional areas within the organization, including but not limited to: State Changes, Releases, Collateral Management ...

Stellantis Financial Services US

QC Analyst

Houston, TX

$23 - $30.75/hr

The QC Analyst will be responsible for performing audits of the various functional areas within the organization, including but not limited to: State Changes, Releases, Collateral Management ...

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

As of Aug 14, 2026, the average hourly pay for senior quality control analyst in Texas is $45.20, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $50.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior quality control analyst, and why are they important?

To thrive as a Senior Quality Control Analyst, you need expertise in laboratory testing, analytical methods, and a strong understanding of regulatory standards, often supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), chromatography software, and relevant certifications such as GMP training are typically required. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies ensure accurate quality assessments, compliance with regulations, and efficient collaboration across teams to maintain product integrity.

How much does a senior quality control analyst earn?

A senior quality control analyst typically earns between $70,000 and $100,000 annually, depending on experience, industry, and location. They often have certifications such as CQE and use tools like laboratory testing equipment, with some roles requiring overtime or shift work.

What are some common challenges faced by senior quality control analysts, and how are they typically addressed?

Senior Quality Control Analysts often encounter challenges such as managing tight deadlines while maintaining high accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. These challenges are typically addressed through effective collaboration with cross-functional teams, ongoing professional development to stay updated with industry regulations, and implementing robust standard operating procedures. Additionally, strong analytical and communication skills help in swiftly resolving issues and ensuring continuous improvement within the quality control process.

What does a senior quality control analyst do?

A Senior Quality Control Analyst is responsible for overseeing and ensuring the quality of products or processes within a company, typically in industries like pharmaceuticals, manufacturing, or food production. They design and implement testing procedures, analyze data, identify defects or inconsistencies, and ensure compliance with regulatory standards. Additionally, they mentor junior analysts, prepare reports, and collaborate with other departments to improve quality systems. Their expertise helps maintain product integrity and supports continuous improvement initiatives.

What are the most commonly searched types of Quality Control Analyst jobs in Texas?

The most popular types of Quality Control Analyst jobs in Texas are:

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

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Senior Quality Control Analyst jobs near you
Infographic showing various Senior Quality Control Analyst job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $94,018 per year, or $45.2 per hour.

Senior Quality Control Analyst & Investigator

Smith & Nephew

Fort Worth, TX • On-site

$23 - $31/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 19 days ago

Smith & Nephew rating

8.1

Company rating: 8.1 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

117th of 539 rated manufacturers

Job description

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.
Senior Quality Control (QC) Analyst & QC Investigator
The Senior QC Analyst & QC Investigator is an experienced, highly skilled individual contributor responsible for leading and executing thorough, compliant laboratory investigations within the Quality Control organization. This role requires deep expertise in identifying true root causes, preventing recurrence through effective CAPA development, and ensuring that all laboratory investigations meet FDA expectations for operations within a sterile drug product manufacturing environment.
The Senior QC Analyst will collaborate closely with chemists, laboratory staff, and cross functional partners to ensure that investigations are completed accurately, efficiently, and on time. This individual will also ensure investigation integrity by preventing "testing into compliance" and by developing sound, scientifically justified retest strategies when appropriate.
What will you be doing?
Laboratory Investigations
  • Lead and conduct comprehensive QC laboratory investigations for OOS, OOT, deviations, atypical results, and invalidations.
  • Apply deep investigative rigor to determine true root cause, using data-driven, scientifically sound methodologies.
  • Ensure all investigations comply with FDA guidance, cGMPs, and expectations for sterile drug-product manufacturing environments.
  • Develop and document robust investigation reports that are accurate, concise, and fully defensible during internal or regulatory audits.
  • Partner with chemists and laboratory teams to gather data, evaluate analytical methods, and review sample preparation and execution details.

CAPA Management
  • Develop effective, preventive, and verifiable CAPAs that address identified root causes and prevent recurrence in the QC laboratory.
  • Facilitate implementation and effectiveness checks of CAPAs across QC operations.
  • Ensure CAPA actions are scientifically justified, feasible, sustainable, and compliant with regulatory expectations.

Compliance & Regulatory Alignment
  • Maintain strong working knowledge of FDA Guidance for Industry related to Out-of-Specification (OOS) results, investigations, and sterile manufacturing environments.
  • Ensure all investigative actions and documentation align with regulatory expectations and withstand regulatory scrutiny.
  • Prevent testing into compliance by ensuring investigative integrity and scientifically justified decision-making.
  • Support audit readiness and provide SME support during regulatory inspections as needed.

Retest and Resample Strategy
  • Develop compliant, scientifically defensible retest, resample, or reanalysis plans when justified by the investigation.
  • Work with analytical teams to ensure retest plans are executed properly and results are understood within proper regulatory context.

Cross-Functional Collaboration
  • Work closely with QC Chemists, Supervisors, QA, Operations, and other teams to ensure timely completion of investigations.
  • Provide coaching and guidance to QC analysts on investigative expectations and best practices.

Serve as an SME for laboratory investigation processes, root-cause analysis tools, and documentation standards.
What will you need to be successful?
Required
  • 8-10 years of extensive experience in Quality Control within the pharmaceutical or biotech industry.
  • Strong experience conducting and documenting QC laboratory investigations.
  • Demonstrated ability to identify true root cause using tools such as 5 Whys, Fishbone, Fault Tree Analysis, and data trending.
  • Deep knowledge of FDA OOS guidance, cGMP for laboratory controls, and requirements for sterile drug product manufacturing.
  • Strong technical understanding of analytical chemistry, method execution, laboratory instrumentation, and data review.
  • Experience developing effective CAPAs and driving implementation.
  • Strong communication skills and the ability to work collaboratively across teams.

Preferred
  • Bachelor's or advanced degree in Chemistry, Microbiology, Biochemistry, or related scientific discipline.
  • Experience supporting regulatory inspections and acting as an SME.
  • Experience in sterile manufacturing environments and aseptic processing quality expectations.

Core Competencies
  • Investigative Rigor & Scientific Judgment
  • Regulatory and Compliance Excellence
  • Collaboration & Teamwork
  • Analytical/Technical Problem Solving
  • Documentation Quality
  • Decision Making with Integrity

U.S. Sponsorship or H1B transfer is not available for this role
You Unlimited.
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
  • Inclusion and Belonging - Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website (https://www.smith-nephew.com/).
  • Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement
  • Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day
  • Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program
  • Flexibility: Hybrid Work Model (For most professional roles)
  • Training: Hands-On, Team-Customized, Mentorship
  • Extra Perks: Discounts on fitness clubs, travel and more!

Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
Stay connected by joining our Talent Community.
We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.
Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N.
Explore our website and learn more about our mission, our team, and the opportunities we offer.

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