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Validation Jobs in Washington, DC (NOW HIRING)

Quality Agents, LLC

Validation Engineer I

Rockville, MD · On-site

Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

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 ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

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 ...

CAI

Computer Systems Validation Engineer

Rockville, MD · On-site

We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...

CAI

Computer Systems Validation Engineer

Rockville, MD

$75K - $106K/yr

We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical ...

Deloitte

System Test and Validation Lead

Mclean, VA · On-site +1

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA ...

Deloitte

System Test and Validation Lead

Rosslyn, VA · On-site +1

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA ...

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All JobsValidation JobsValidation Jobs in Washington, DC

Validation information

See Washington, DC salary details

$25

$58

$88

How much do validation jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for validation in Washington, DC is $58.87, according to ZipRecruiter salary data. Most workers in this role earn between $44.62 and $71.59 per hour, depending on experience, location, and employer.

What is a validation job?

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 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 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 does a validation specialist do?

A validation specialist is responsible for ensuring that processes, equipment, and systems meet regulatory standards and quality requirements. They develop, execute, and document validation protocols, often working with industries like pharmaceuticals, biotech, or manufacturing, and may use tools such as validation software and perform risk assessments. Certification and attention to detail are important in this role.

What are the most commonly searched types of Validation jobs in Washington, DC?

The most popular types of Validation jobs in Washington, DC are:

Validation jobs near you
Infographic showing various Validation job openings in Washington, DC as of August 2026, with employment types broken down into 79% Full Time, 6% Part Time, 2% Temporary, and 13% Contract. Highlights an 88% In-person, 4% Hybrid, and 8% Remote job distribution, with an average salary of $122,493 per year, or $58.9 per hour.

Validation Engineer / Validation Specialist

Rockville, MD • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Posted 25 days ago

Job description

Position: Validation Engineer / Validation Specialist
Location: Maryland
Duration: Long Term

Job Overview

We are seeking an experienced Validation Engineer / Validation Specialist to support equipment, utility, and process qualification activities within a GMP pharmaceutical/biotechnology manufacturing environment. The ideal candidate will prepare and execute IQ, OQ, PQ, and Requalification (RQ) protocols, generate validation reports, develop technical documentation, and ensure compliance with cGMP and Good Documentation Practices (GDP).

Key Responsibilities

  • Prepare, execute, and document IQ, OQ, PQ, and Requalification (RQ) protocols for equipment and utilities.
  • Generate qualification reports, SOPs, specifications, methods, and other validation documentation.
  • Develop acceptance criteria based on industry standards, manufacturer recommendations, user requirements, and cGMP guidelines.
  • Perform thermal mapping studies using Kaye AVS or Veriteq data loggers.
  • Analyze validation data and verify compliance with acceptance criteria.
  • Investigate, document, and resolve deviations associated with qualification studies.
  • Support commissioning, Factory Acceptance Testing (FAT), and Site Acceptance Testing (SAT).
  • Prepare technical reports, gap assessments, and risk assessments.
  • Provide technical support for troubleshooting manufacturing equipment and systems.
  • Perform technical reviews of qualification documents.
  • Support internal and external audit readiness activities.

Required Qualifications

  • Bachelor's degree in Engineering or a related scientific discipline with a minimum of 4 years of validation experience, or 8+ years of relevant validation experience in lieu of a degree.
  • Experience working in GMP pharmaceutical or biotechnology manufacturing environments.
  • Hands-on experience with Equipment Qualification (IQ/OQ/PQ/RQ) activities.
  • Knowledge of cGMP regulations and Good Documentation Practices (GDP).
  • Experience with aseptic manufacturing processes.
  • Familiarity with Kaye AVS or Veriteq thermal mapping systems.
  • Working knowledge of cleanrooms, sterilization equipment, HVAC, WFI, RO, CCA, computerized systems, and isolator technology.
  • Experience with Microsoft Office, EDMS, LIMS, and related documentation systems.
  • Strong technical writing, communication, organizational, and project management skills.
  • Ability to work independently and collaboratively in a cross-functional environment.
  • Knowledge of maintenance and calibration procedures is preferred.