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Pharmaceutical Validation Engineer Jobs (NOW HIRING)

Sigan America LLC

Validation Engineer

Ottawa, IL · On-site

$90K - $100K/yr

Senior Validation Engineer Location: Ottawa, Illinois Employment Type: Full-Time About the Position ... The ideal candidate has a strong technical background in pharmaceutical, medical device, cosmetic ...

RD Partners

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

R&D Partners is seeking to hire a Validation Engineer in Tucson, AZ . Your main responsibilities as ... We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ...

Actalent

Validation Engineer

Paramus, NJ

Validation Engineer This role focuses on developing and executing validation, cleaning, and ... Experience in pharmaceutical, medical device, or broader life science manufacturing environments.

Stark Pharma Solutions Inc

MD · On-site

I am working on Validation Engineer right now. Please send me your updated resume if you have ... Hands-on experience in GMP pharmaceutical or biotechnology manufacturing . * Strong knowledge of IQ ...

kindeva

Validation Engineer II

Maryland Heights, MO · On-site

The Impact You Will Make The Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site.

kindeva

Validation Engineer II

Maryland Heights, MO · On-site

The Impact You Will Make The Floater Validation Engineer II provides validation engineering support across two pharmaceutical aseptic manufacturing facilities and one inspection and packaging site.

Valspec

Validation Engineer (CSV)

Seattle, WA

Lead Validation Engineer (CSV / DeltaV) Valspec | Seattle, WA Full-Time | Hybrid Client Site ... Valspec partners with pharmaceutical and biotechnology manufacturers to deliver compliant, reliable ...

Valspec

Validation Engineer (CSV)

Redmond, WA

Lead Validation Engineer (CSV / DeltaV) Valspec | Seattle, WA Full-Time | Hybrid Client Site ... Valspec partners with pharmaceutical and biotechnology manufacturers to deliver compliant, reliable ...

Pinnaql

Jr Validation Engineer

New Albany, OH · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

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Pharmaceutical Validation Engineer information

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$22

$51

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How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for pharmaceutical validation engineer 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 does a pharmaceutical validation engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation engineer?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What are the most common challenges a pharmaceutical validation engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.

What is the difference between Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

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Pharmaceutical Validation Engineer jobs near you
Infographic showing various Pharmaceutical Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Katalyst Healthcares and Lifesciences

Bothell, WA • On-site

Other

Posted 3 days ago

New

Job description

Summary :
We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized system validation within a GMP-regulated pharmaceutical environment. This role requires strong knowledge of validation lifecycle activities, regulatory compliance, documentation, and cross-functional collaboration.
Roles & Responsibilities :
  • Execute and support validation lifecycle activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Develop, review, and approve validation protocols, test scripts, summary reports, and related GMP documentation.
  • Perform equipment qualification for manufacturing, packaging, utilities, and laboratory systems.
  • Support process validation, cleaning validation, and revalidation activities for pharmaceutical manufacturing processes.
  • Conduct impact assessments for change controls, deviations, CAPA, and non-conformance investigations.
  • Collaborate with Quality Assurance, Manufacturing, Engineering, and Regulatory teams to ensure compliance with validation requirements.
  • Ensure validation documentation aligns with FDA, cGMP, GxP, 21 CFR Part 11, and data integrity requirements.
  • Participate in commissioning and qualification activities for new equipment and facility expansions.
  • Review calibration, maintenance, and qualification records for compliance readiness.
  • Support internal/external audits and regulatory inspections by providing validation documentation and technical expertise.
  • Maintain validation master plans, SOPs, and validation schedules.

Education & Experience :
  • Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related field.
  • 5+ years of validation experience in pharmaceutical, biotech, or life sciences industry.
  • Strong experience in IQ/OQ/PQ, process validation, cleaning validation, CSV, and equipment qualification.
  • Knowledge of FDA regulations, cGMP, GAMP 5, 21 CFR Part 11, ALCOA+, and validation lifecycle methodologies.
  • Experience with deviations, CAPA, change controls, and risk assessments.
  • Excellent documentation, analytical, and problem-solving skills.
  • Strong communication skills and ability to work cross-functionally in a fast-paced environment.
  • Experience with sterile manufacturing, aseptic processing, or biologics is a plus.
  • Familiarity with validation management systems such as TrackWise, Veeva, Kneat, MasterControl, or ValGenesis.
  • Prior experience supporting regulatory inspections or audit readiness initiatives.

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