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Quality Validation Jobs (NOW HIRING)

CIS International LLC

PR

Lead and support investigations, deviations, and CAPAs, providing technical expertise to resolve complex quality, validation, and manufacturing issues. * Develop, implement, and continuously improve ...

Experis

Silicon Validation Engineer 3

Redmond, WA · On-site

$64/hr

Maintain and run silicon system regressions, ensuring high-quality validation processes. What's Needed? * Minimum of 3+ years of hands-on experience in silicon validation, testing, or debugging.

Serán BioScience

Senior Validation Engineer

Bend, OR · On-site

Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing * Fundamental understanding of process equipment ...

RFA Engineering

Quality/Test Engineer

Chillicothe, IL · On-site

$70K - $95K/yr

Support quality, validation, and testing activities for engine, powertrain, and off-highway equipment programs. * Develop and execute test plans, test procedures, and validation activities. * Collect ...

CIS International LLC

PR

Lead and support investigations, deviations, and CAPAs, providing technical expertise to resolve complex quality, validation, and manufacturing issues. * Develop, implement, and continuously improve ...

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Quality Validation information

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How much do quality validation jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for quality validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are some common challenges faced in a quality validation role and how can they be addressed?

Professionals in Quality Validation often encounter challenges such as managing tight project deadlines, ensuring compliance with ever-evolving regulatory standards, and effectively communicating with cross-functional teams. Addressing these challenges involves strong organizational skills, continuous learning about industry regulations, and fostering collaboration between departments like manufacturing, R&D, and quality assurance. Staying proactive and maintaining thorough documentation also helps mitigate risks and improve validation processes.

What is quality validation?

Quality Validation is a process used in various industries, especially in manufacturing, pharmaceuticals, and software development, to ensure that products, processes, or systems meet predefined quality standards and regulatory requirements. It involves planned and systematic activities such as testing, documentation, and reviews to confirm that the final output consistently meets the intended purpose. Quality Validation helps organizations minimize errors, enhance reliability, and build customer trust by ensuring that products are both safe and effective before they reach the market.

What are the key skills and qualifications needed to thrive as a quality validation specialist, and why are they important?

To excel as a Quality Validation Specialist, you need a solid understanding of quality assurance principles, regulatory compliance, and validation methodologies, often supported by a degree in a scientific or engineering field. Familiarity with validation protocols, statistical analysis software, and quality management systems (QMS) is typically required, along with certifications like Six Sigma or GMP training. Attention to detail, problem-solving, and effective communication are crucial soft skills for identifying issues and ensuring compliance across teams. These competencies are vital for maintaining product safety, regulatory adherence, and continuous improvement within quality-driven industries.

What is the difference between Quality Validation vs Quality Assurance?

AspectQuality ValidationQuality Assurance
Primary FocusEnsuring products meet user needs and specifications through testing and validationImplementing processes to prevent defects and improve quality systems
ActivitiesValidation testing, product verification, compliance checksProcess audits, quality system development, preventive measures
CredentialsOften requires technical certifications and testing experienceQuality management certifications like ISO, Six Sigma
Work EnvironmentLaboratories, testing facilities, production linesQuality departments, process improvement teams

While both roles aim to ensure product quality, Quality Validation focuses on testing and verifying that products meet specifications, whereas Quality Assurance emphasizes establishing processes to prevent defects and improve overall quality systems.

More about Quality Validation jobs
What are the most commonly searched types of Quality Validation jobs? The most popular types of Quality Validation jobs are:
What states have the most Quality Validation jobs? States with the most job openings for Quality Validation jobs include:
What job categories do people searching Quality Validation jobs look for? The top searched job categories for Quality Validation jobs are:
Quality Validation jobs near you
Infographic showing various Quality Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Qualification & Validation Engineer II - capital projects

CIS International LLC

PR

Full-time, Contractor

Posted 12 days ago

Job description

Summary:
Commissioning and Qualification (C&Q) contracted services to support capital projects for the Engineering department of a pharmaceutical manufacturing industry in Puerto Rico.
Responsibilities:
  • Provide technical leadership for commissioning, qualification, and computer system validation activities, including:
    • Leading and executing end-to-end qualification and lifecycle management of facilities, utilities, manufacturing equipment, process systems, and computerized systems.
    • Planning, coordinating, and delivering qualification and validation project milestones within scope, timeline, and budget constraints.
    • Developing, reviewing, approving, and executing validation lifecycle documentation, including Validation Master Plans, User Requirements Specifications (URS), Functional and Design Specifications, Risk Assessments, Commissioning Plans, IQ/OQ/PQ protocols, and summary reports.
    • Directing protocol execution activities, including data collection, field sampling, data trending, statistical analysis, deviation assessment, root cause investigations, and implementation of corrective actions.
    • Monitoring, tracking, and communicating validation project status, risks, and deliverables to project teams and leadership.
  • Develop and scientifically justify validation strategies, acceptance criteria, sampling plans, and protocol designs based on risk management principles, process understanding, and industry best practices.
  • Evaluate and document the impact of change controls on qualified systems, validated processes, facilities, utilities, and computerized systems, ensuring compliance with site and regulatory requirements.
  • Lead and support investigations, deviations, and CAPAs, providing technical expertise to resolve complex quality, validation, and manufacturing issues.
  • Develop, implement, and continuously improve validation procedures, standards, policies, and lifecycle management practices aligned with regulatory expectations and industry trends.
  • Maintain compliance with current global regulatory requirements and industry guidance, including but not limited to:
    • 21 CFR Parts 210, 211, and 11
    • EU GMP Annex 11 and Annex 15
    • ICH Q8, Q9, and Q10
    • ISPE Baseline Guides and GAMP 5
    • Applicable domestic and international regulatory standards
  • Manage multiple high-priority projects simultaneously, balancing competing demands while consistently meeting aggressive timelines and business objectives.
  • Perform other duties and special projects as assigned.
Requirements:
  • Bachelor's degree in Engineering, Biology, Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • 3-5 years’ experience in pharmaceutical or regulated manufacturing environment; ideally, the candidate will have previous Oral Solid Dose (OSD) manufacturing experience.
Work Methodology:
  • Professional services agreement (independent contractor)
  • Full time job
  • Full on site job in Vega Baja, Puerto Rico
  • Languages: Spanish and English
  • Type of industry: Pharmaceutical
  • Expected hiring date:  August 2026
  • Project term: 6-12 months with potential extensions
  • Amount of openings: 4
  • Administrative shift, wiling to support non-admin hours