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Validation Manager Jobs in Virginia (NOW HIRING)

Guidehouse

Model Validation Lead

Mclean, VA

Advise clients on model risk management, AI governance, and responsible AI practices * Mentor ... Experience validating ML, statistical, and predictive models in regulated or highrisk environments

Guidehouse

Model Validation Lead

Mclean, VA · On-site

Advise clients on model risk management, AI governance, and responsible AI practices * Mentor ... Experience validating ML, statistical, and predictive models in regulated or high-risk environments

Guidehouse

Model Validation Lead

Arlington, VA

Advise clients on model risk management, AI governance, and responsible AI practices * Mentor ... Experience validating ML, statistical, and predictive models in regulated or highrisk environments

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

Position Summary Validation Engineer II will be responsible for leading the commissioning ... Interpersonal skills to manage interactions and achieve results across a range of functions within ...

Civica Rx

Validation Engineer II (377)

Petersburg, VA · On-site

Position Summary Validation Engineer II will be responsible for leading the commissioning ... Interpersonal skills to manage interactions and achieve results across a range of functions within ...

BeiGene USA

Senior Engineer I, Validation

Hopewell, VA · On-site

May manage validation consultants on a large project basis, as needed. * Leading and Managing projects for the validation of equipment, processes, and products to meet all safety, quality, regulatory ...

CAI

Senior Validation Engineer

Charlottesville, VA

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

CAI

Senior Validation Engineer

Charlottesville, VA

$87K - $94K/yr

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

Dover Corporation

Validation Coordinator Location: Richmond What we are looking for: This position is part of the ... Ability to interact with associates/supervisor/managers * Well-developed interpersonal skills How ...

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All JobsValidation Manager JobsValidation Manager Jobs in Virginia

Validation Manager information

See Virginia salary details

$47.1K

$104.5K

$159.1K

How much do validation manager jobs pay per year?

As of Jun 27, 2026, the average yearly pay for validation manager in Virginia is $104,511.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $130,900.00 per year, depending on experience, location, and employer.

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

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the role of a validation manager?

A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and utilizing validation tools. Their role is critical in industries like pharmaceuticals, manufacturing, and healthcare to ensure safety and efficacy.

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

A Validation Manager typically earns a salary that can reach or exceed $10,000 per month, especially with experience and industry expertise. This role involves overseeing validation processes in industries like pharmaceuticals or manufacturing, often requiring strong technical skills and certifications but not necessarily a college degree.

What jobs in the US pay 300,000 a year?

Validation Managers in industries such as pharmaceuticals, biotechnology, and manufacturing can earn salaries approaching or exceeding $300,000 annually, especially with extensive experience, advanced certifications, and leadership responsibilities. High-level roles in finance, law, and executive management also frequently reach or surpass this salary level. Compensation varies based on location, company size, and individual expertise.

What Is a Validation Manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

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

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

What jobs pay 500,000 a year in the US?

Validation Managers typically do not earn $500,000 annually; such high salaries are more common in executive roles like CEOs, CFOs, or specialized high-level professionals in finance, law, or technology. Senior executives and certain specialized roles with significant responsibilities and experience can reach or exceed this income level, often including bonuses and stock options. Compensation varies widely based on industry, company size, and geographic location.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

What are Validation Managers?

Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.
More about Validation Manager jobs
What are the most commonly searched types of Validation jobs in Virginia? The most popular types of Validation jobs in Virginia are:
What are popular job titles related to Validation Manager jobs in Virginia? For Validation Manager jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Validation Manager jobs in Virginia look for? The top searched job categories for Validation Manager jobs in Virginia are:
What cities in Virginia are hiring for Validation Manager jobs? Cities in Virginia with the most Validation Manager job openings:
Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Virginia as of June 2026, with employment types broken down into 4% As Needed, 72% Full Time, 2% Part Time, 4% Temporary, 16% Contract, and 2% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $104,511 per year, or $50.2 per hour.
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 402 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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