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Validation Engineer Jobs (NOW HIRING)

Pinnaql

Validation Engineer

Holly Springs, NC · On-site

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

Veg Group

Validation Engineer

Greenville, NC · On-site

$75 - $95/hr

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

Pinnaql

Validation Engineer

Cincinnati, OH · On-site

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

Pinnaql

Validation Engineer

New Albany, OH · On-site

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

Pinnaql

Validation Engineer

Wilson, NC · 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 ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

$85 - $120/hr

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 ...

Pinnaql, Inc.

$85 - $130/hr

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 ...

Pinnaql

Validation Engineer

Atlanta, GA · On-site

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

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 a Validation Engineer: · Develop, write, review, and execute process validation/process ...

Pinnaql

Validation Engineer

Wilson, NC

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 ...

Veg Group

Validation Engineer

Cincinnati, OH · On-site

$70 - $90/hr

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

Verhaert New Products & Services NV

WI · On-site

$80 - $100/hr

Validation Engineer - Automotive Werk mee aan de volgende generatie voertuigtechnologie. Als Validation Engineer binnen onze consultingactiviteiten help je bij het valideren van complexe ...

Onsite Personnel LLC

Validation Engineer

Newtown, PA · On-site

Validation Engineer: Support site commissioning and qualification, which includes but is not limited to the following: equipment, utilities, cleaning, process, assay qualifications. Ensuring the ...

JSat Automation

Validation Engineer

Glendale, CA · On-site

The Validation Engineer will be responsible for the following. * Develop, approve, and execute process validation studies and protocols for cell and gene therapy manufacturing. * Design and develop ...

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Validation Engineer information

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How much do validation engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for 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 is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

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

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

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

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Concord, NC • On-site

Contractor

Re-posted 26 days ago

Job description

Job Title: Validation Engineer
Location: Concord, NC
Duration: Long Term

Job Summary

We are seeking a motivated and detail-oriented Validation Engineer to support validation activities within a GMP-regulated biopharmaceutical manufacturing environment. The Validation Engineer will be responsible for equipment qualification, process validation, utility validation, and cleaning validation activities to ensure compliance with FDA, cGMP, and industry standards.

The ideal candidate will collaborate with Manufacturing, Quality Assurance, Engineering, and Regulatory teams to support production operations, maintain validated systems, and ensure regulatory compliance across the facility.

Key Responsibilities

  • Develop, execute, and review validation protocols and reports including IQ, OQ, and PQ documentation
  • Support equipment qualification activities for biopharmaceutical manufacturing equipment and laboratory systems
  • Perform process validation for upstream and downstream manufacturing processes
  • Execute cleaning validation and utility qualification activities including HVAC, purified water, compressed gases, and cleanroom systems
  • Ensure compliance with FDA, cGMP, GDP, and company quality standards
  • Support computerized systems validation (CSV) activities when required
  • Participate in deviation investigations, root cause analysis, CAPA, and change control processes
  • Collaborate with cross-functional teams during equipment installation, commissioning, and technology transfer projects
  • Maintain validation lifecycle documentation including SOPs, Validation Master Plans (VMP), and risk assessments
  • Assist during internal audits and regulatory inspections by providing validation documentation and technical support
  • Identify and implement continuous improvement opportunities within validation and manufacturing processes

Required Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related field
  • 3+ years of validation experience in biopharmaceutical, pharmaceutical, or regulated manufacturing industries
  • Strong understanding of cGMP, FDA regulations, and validation principles
  • Experience with IQ/OQ/PQ protocol execution and report generation
  • Knowledge of process validation, cleaning validation, and utility qualification
  • Familiarity with deviation management, CAPA, and change control systems
  • Strong technical writing and documentation skills
  • Excellent communication, analytical, and problem-solving abilities