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Validation Jobs in Virginia (NOW HIRING)

Guidehouse

Model Validation Lead

Mclean, VA

You will lead model validation efforts supporting missioncritical use cases across defense and federal financial domains, ensuring models are sound, explainable, compliant, and operationally fit for ...

Guidehouse

Model Validation Lead

Mclean, VA · On-site

You will lead model validation efforts supporting mission-critical use cases across defense and federal financial domains, ensuring models are sound, explainable, compliant, and operationally fit for ...

Guidehouse

Model Validation Lead

Arlington, VA

You will lead model validation efforts supporting missioncritical use cases across defense and federal financial domains, ensuring models are sound, explainable, compliant, and operationally fit for ...

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

Position Summary Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) for a newly announced facility expansion for biologics that includes a ...

CAI

Senior Validation Engineer

Charlottesville, VA

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

CAI

Senior Validation Engineer

Charlottesville, VA

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

BeiGene USA

Senior Engineer I, Validation

Hopewell, VA · On-site

Supports Validation objectives, whilst adhering to regulatory compliance and achieving commercial success. This is a site-based position supporting the facility and will required gowning into the ...

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How much do validation jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for validation in Virginia is $51.55, according to ZipRecruiter salary data. Most workers in this role earn between $39.09 and $62.69 per hour, depending on experience, location, and employer.

What is a validation job?

A validation job involves verifying that products, processes, or systems meet specified standards and requirements. It often includes tasks such as testing, documentation, and compliance checks, especially in industries like pharmaceuticals, manufacturing, and technology. Skills in quality assurance, attention to detail, and familiarity with validation protocols are typically required.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What is the 3 month rule for jobs?

In validation roles, the 3 month rule often refers to a probationary period during which an employee's performance and fit for the position are assessed. This period typically allows employers to evaluate skills, adherence to procedures, and reliability before confirming permanent employment or considering further training. It is common for companies to set this timeframe to ensure quality and compliance in validation processes.

What jobs pay $10,000 a month without a degree?

Validation roles typically do not pay $10,000 a month without specialized skills or experience. High-paying jobs that can reach this level without a degree often include sales, real estate, or certain entrepreneurial ventures, but they usually require strong skills, certifications, or a proven track record. Most roles with such income levels rely on performance-based compensation rather than formal education alone.

What engineers make $500,000?

Senior engineers in specialized fields such as software, petroleum, or aerospace engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. High-level roles typically require extensive experience, advanced skills, and sometimes professional certifications or advanced degrees.

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 or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What are validation jobs?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Virginia? The most popular types of Validation jobs in Virginia are:
What cities in Virginia are hiring for Validation jobs? Cities in Virginia with the most Validation job openings:
Validation jobs near you
Engineer II, Validation

Engineer II, Validation

Thermo Fisher Scientific

Middletown, VA • On-site

Full-time

Posted 2 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 405 frontline employees who took The Breakroom Quiz

188th of 521 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Warehouse, Will work with hazardous/toxic materials
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Thermo Fisher Scientific's Clinical Diagnostic Reagents (CDR) group is seeking a Validation Engineer to support planning and execution of validation activities for clinical diagnostic reagent manufacturing within a cGMP, FDA, and ISO 13485 regulated environment. This role requires full onsite presence to support equipment, process, and system validation activities.
This position will assist in development, execution, and documentation of validation protocols and reports while ensuring alignment with regulatory and site requirements. The role includes supporting periodic reviews and conducting gap assessments to ensure continued compliance with validation standards and site procedures. This position works under the guidance of senior validation engineers and reports directly to the Senior Manager of Engineering for the facility.
Location: Middletown, VA. Relocation assistance is NOT provided.
KEY RESPONSIBILITIES:
  • Support creation and execution of validation master plans for facility equipment, systems, and processes
  • Author, revise, and execute validation protocols (IQ, OQ, PQ) and associated reports
  • Participate in periodic validation reviews and gap assessments to ensure ongoing compliance with regulatory and site standards
  • Assist in identifying validation gaps and support development of remediation plans
  • Analyze validation data to verify systems and processes meet defined acceptance criteria
  • Collaborate cross-functionally with Engineering, Quality, Manufacturing, and other departments to coordinate validation activities
  • Support deviation investigations, root cause analysis, and implementation of corrective actions
  • Maintain validation documentation in accordance with site quality systems
  • Support change control activities related to validated systems
  • Assist in calibration coordination and verification activities

REQUIREMENTS/QUALIFICATIONS:
  • Bachelor's degree in Engineering, Life Sciences, Chemistry or related technical field
  • 2-3 years of validation experience in GMP/regulated industry (Medical Device or Pharmaceutical preferred)
  • Familiarity with cGMP, FDA regulations, and industry standards (ISO, GAMP5)
  • Strong technical writing skills for validation documentation
  • Experience with IQ/OQ/PQ protocols and execution
  • Proficiency in risk based quality tools (FMEA, Risk Analysis, RCA,CAPA)
  • Experience managing validation projects independently
  • Knowledge of calibration and metrology principles
  • Experience with automation systems and computer system validation
  • Ability to work in cleanroom environments when required
  • Experience with quality management systems and documentation
  • Knowledge of statistical analysis and process control methods
  • Must be legally authorized to work in the United States without sponsorship
  • Must be able to pass a comprehensive background check, which includes a drug screening

Core Competencies
  • Strong data analysis and problem-solving capabilities
  • Clear verbal and written communication skills
  • Proficient in Microsoft Office applications
  • Effective interpersonal skills for team collaboration
  • Ability to manage multiple projects
  • Consistent record of completing projects on schedule in a deadline-oriented environment

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