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System Validation Jobs in Washington, DC (NOW HIRING)

Bluestone Logic

Test Engineer - Senior

Washington, DC · On-site

The Senior Test Engineerwill be supporting the Defense Information Systems Agency (DISA) and leads test strategy, automation, and performance validation efforts for Spectrum XXI software suite ...

Valspec

CSV Lead

Rockville, MD

$104K - $137K/yr

Valspec--a global provider of system validation and lifecycle services--provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999 ...

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System Validation information

See Washington, DC salary details

$33

$58

$85

How much do system validation jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for system validation in Washington, DC is $58.67, according to ZipRecruiter salary data. Most workers in this role earn between $44.09 and $72.98 per hour, depending on experience, location, and employer.

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

AspectSystem ValidationQuality Assurance Specialist
CredentialsTypically requires engineering or technical degrees, certifications like ISTQB or ISO auditorRequires quality management certifications, such as ASQ CQE or Six Sigma
Work EnvironmentFocuses on testing and verifying systems, often in manufacturing, software, or medical device industriesInvolves process audits, documentation, and compliance across various industries
Employer & Industry UsageUsed in regulated industries like healthcare, aerospace, and software developmentCommon in manufacturing, software, and service industries for maintaining quality standards

System Validation and Quality Assurance Specialists both ensure product quality but differ in scope. System Validation primarily verifies that systems meet specifications, while Quality Assurance focuses on process improvement and compliance. Understanding these roles helps in choosing the right career path or hiring the right professional.

Is computer system validation a good field?

Computer system validation is a specialized field within quality assurance and regulatory compliance, primarily in industries like pharmaceuticals and biotech. It involves ensuring that computer systems meet regulatory standards through documentation, testing, and validation protocols, often requiring knowledge of GxP guidelines and validation tools. The field offers steady demand and opportunities for growth with relevant certifications and technical skills.

What is the job description of system validation?

System validation involves testing and verifying that a system or product meets specified requirements and functions correctly in its intended environment. It includes designing validation protocols, executing tests, analyzing results, and ensuring compliance with industry standards, often using tools like test management software. Professionals in this role need strong analytical skills and knowledge of quality assurance processes.
System Validation jobs near you
Infographic showing various System Validation job openings in Washington, DC as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $122,034 per year, or $58.7 per hour.

Validation Engineer IV

Rockville, MD • On-site

Quality Agents, LLC
Biotechnology Research and Development • 11 - 50 employees
Learn more about Quality Agents, LLCexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The Validation Engineer will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the Validation Engineer must be approved by the client.
Responsibilities include:
  • Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents.
  • Travel to various client sites and work independently to complete tasks.
  • Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites.
  • Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion.
  • Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards.
  • Conducts temperature mapping studies, including the operation of Kaye dataloggers, or equivalent.
  • Review and approve documented test results and maintain records for later analysis.
  • Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems.
  • Able to read P&IDs, isometric drawings, and As-built drawings.

Skill Level and Requirements:
  • Ability to problem solve and troubleshoot.
  • Technical writing ability and use of Microsoft Word, Excel, Power point, and Project
  • Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired.
  • Experience using statistical tools is a plus to analyze data captured during validation studies.

Minimum Requirements:
  • BS in a technical discipline (Engineering, chemistry, microbiology, biology)
  • 7+ years of experience in at least one of the following areas: equipment/utility qualifications, process validation, analytical method validation, or cleaning validation.
  • Current driver's license and auto insurance

Quality Agents offers a full suite of benefits for full-time employees including:
  • Health, dental and vision insurance
  • Life, AD&D and disability Insurance
  • Health savings account for participants in our health plan
  • 401k retirement plan
  • Paid time off
  • Paid holidays

Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.

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