1

Validation Associate Jobs in Texas (NOW HIRING)

Senior Engineer, Process Validation

Dallas, TX · On-site +1

$100K - $130K/yr

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

... Validates associates are working safe and free of clutter • Funnels non-MOD activities (e.g., customer complaints, management approvals, and other run the business activities) to appropriate non ...

Administrative Associate

Austin, TX · On-site

$17.25 - $21.50/hr

DOE Mission/ Position Description Summary The mission of the Administrative Associate at HVJ South ... Valid drivers license and current automobile insurance * Ability to work well indepndently and in ...

Associate Dentist

San Antonio, TX · On-site

$250K - $350K/yr

Exciting Opportunity for an Associate Dentist! Join our advanced comprehensive dentistry practice ... Valid dental license in Texas * Strong clinical skills with a passion for patient-centered care

Exciting Opportunity for an Associate Dentist! Join our advanced comprehensive dentistry practice ... Valid dental license in Texas * Strong clinical skills with a passion for patient-centered care

Associate Dentist

San Antonio, TX · On-site

$250K - $350K/yr

Exciting Opportunity for an Associate Dentist! Join our advanced comprehensive dentistry practice ... Valid dental license in Texas * Strong clinical skills with a passion for patient-centered care

Exciting Opportunity for an Associate Dentist! Join our advanced comprehensive dentistry practice ... Valid dental license in Texas * Strong clinical skills with a passion for patient-centered care

Sales Associate

Corpus Christi, TX · On-site

$11 - $14.75/hr

Description Principle BMW of Corpus Christi Sales Associate Who You Are Principle BMW of Corpus ... Valid state of residence driver's license. * Bachelor's degree preferred.

next page

Showing results 1-20

Validation Associate information

See Texas salary details

$21

$48

$72

How much do validation associate jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for validation associate in Texas is $48.44, according to ZipRecruiter salary data. Most workers in this role earn between $36.73 and $58.89 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Validation Associate, and why are they important?

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

How much does a validation specialist make in the US?

A validation specialist in the US typically earns between $60,000 and $85,000 annually, depending on experience, industry, and location. Entry-level roles may start around $50,000, while experienced professionals with certifications can earn over $100,000. Skills in quality assurance, regulatory compliance, and validation tools are often required for higher salaries.

What job makes $10,000 a month without a degree?

A Validation Associate typically does not earn $10,000 a month without a degree; such high earnings are uncommon for this role. Generally, jobs that can pay $10,000 monthly without a degree include specialized sales, real estate brokers, certain tech sales positions, or skilled trades with experience and commissions. These roles often require strong skills, certifications, or extensive experience rather than formal degrees.

Is QC a high paying job?

Quality Control (QC) roles, including validation associates, typically offer salaries that are average or slightly above average compared to other entry-level positions in manufacturing and healthcare industries. Compensation varies based on experience, location, and industry, with specialized skills and certifications potentially increasing earning potential.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What are Validation Associates?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

Is Associate the lowest position?

In the role of Validation Associate, this position is typically an entry-level or early-career role within the validation or quality assurance departments. It is often the starting point before advancing to higher roles such as Senior Validation Associate or Validation Specialist, depending on the company's structure and experience required. The lowest position in a validation or quality team may vary by organization but often begins with entry-level titles like Validation Associate or Technician.

How does a Validation Associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.
What are the most commonly searched types of Validation jobs in Texas? The most popular types of Validation jobs in Texas are:
What are popular job titles related to Validation Associate jobs in Texas? For Validation Associate jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in Texas look for? The top searched job categories for Validation Associate jobs in Texas are:
What cities in Texas are hiring for Validation Associate jobs? Cities in Texas with the most Validation Associate job openings:
Senior Engineer, Process Validation

Senior Engineer, Process Validation

Danaher

Dallas, TX • On-site, Remote

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago


Danaher rating

7.5

Company rating: 7.5 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time.

Learn about the Danaher Business System which makes everything possible.

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines.

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote.

In this role, you will have the opportunity to:

  • Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
  • Lead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping.
  • Drive risk-based approaches using tools such as pFMEA, risk ranking, and criticality assessments and apply statistical tools to evaluate process performance, including but not limited to process capability, trend analysis and control charts and DOE) interpretation.
  • Serve as a technical SME for process validation with external clients, across internal teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.
  • Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design

The essential requirements of the job include:

  • Bachelor or master degree in engineering and 5+ years of experience
  • Prior experience in leading process development, engineering, and deliverables across all three stages of process validation in biologics/small and large molecules manufacturing train using statistical analysis, risk assessment, and process improvement tools required.
  • Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
  • Proficiency in technical writing with deviation investigations, root cause analysis, and risk assessments.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 15% to site to support validation project executions, routine inspections, audits, and client visits.

It would be a plus if you also possess previous experience in:

  • Packaging and shipping validation of final product container closure configurations.
  • Client facing roles such as prior experience in a CDMO environment

Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Aldevron we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Aldevron can provide.

The annual salary range for this role is $100,000 to $130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

#LI-PF1

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


What Danaher employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Danaher logo

About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984