1

Computer Validation Jobs in Virginia (NOW HIRING)

Bachelor's degree in Mathematics, Statistics, Computer Science, Engineering, Economics, or a related quantitative field * FIVE (5) or more years of experience in model validation, model risk ...

Bachelor's degree in Mathematics, Statistics, Computer Science, Engineering, Economics, or a related quantitative field * FIVE (5) or more years of experience in model validation, model risk ...

Bachelor's degree in Mathematics, Statistics, Computer Science, Engineering, Economics, or a related quantitative field * FIVE (5) or more years of experience in model validation, model risk ...

The Computer Operator III processes a range of scheduled routines. In addition to operating the ... M processor, Validator, Key Enabling Entity Bundle (KEEB) Validator, Training Resource ...

Computer Vision Engineer

Sterling, VA · On-site

$110K - $130K/yr

As a Computer Vision Engineer, you will: * Drive the architecture, development, and deployment of ... Define and maintain best practices for system design, testing, and validation of vision pipelines ...

Computer Scientist - Mid ***This position requires an active TS/Sensitive Compartmental Information ... Uses argument evaluation and validated analytic methodologies to challenge differing perspectives.

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

next page

Showing results 1-20

Computer Validation information

See Virginia salary details

$10

$53

$85

How much do computer validation jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for computer validation in Virginia is $53.85, according to ZipRecruiter salary data. Most workers in this role earn between $41.49 and $63.85 per hour, depending on experience, location, and employer.

Can computer engineers make $500,000?

Computer validation professionals typically do not earn $500,000 annually, as this level of compensation is uncommon in the field. High salaries may be possible for senior roles, especially in biotech or pharmaceutical industries, or with extensive experience, specialized skills, and leadership responsibilities. Most salaries for computer validation roles range from $70,000 to $150,000 per year.

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

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What is the salary of a CSV engineer?

A CSV (Computer System Validation) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications. Senior roles or those with specialized skills in validation tools and regulatory compliance may earn higher salaries.

Is computer system validation a good field?

Computer validation professionals ensure that computer systems in regulated industries meet quality and compliance standards, often working with tools like GxP and validation protocols. The field offers steady demand, especially in pharmaceuticals and biotech, and requires knowledge of regulatory requirements and validation processes. It can be a rewarding career for those interested in quality assurance, compliance, and technical problem-solving.

Is CSV a skill?

In the context of computer validation, familiarity with CSV (comma-separated values) files is considered a useful technical skill, as it involves working with data formats and data management tools. Proficiency in handling CSV files can support tasks such as data import/export, validation, and reporting. However, CSV itself is a data format, not a standalone skill, but understanding how to work with it is valuable for validation professionals.
What are popular job titles related to Computer Validation jobs in Virginia? For Computer Validation jobs in Virginia, the most frequently searched job titles are:
What cities in Virginia are hiring for Computer Validation jobs? Cities in Virginia with the most Computer Validation job openings:
Engineer II, Validation

Full-time

Posted 24 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 401 frontline employees who took The Breakroom Quiz

187th of 519 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

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom