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Pharmaceutical Validation Engineer Jobs in Virginia

Doist

Validation Engineer

Elkton, VA · On-site

$85 - $110/hr

Pharmaceutical facilities * Utilities * Equipment Project & Team Management * Plan and coordinate ... Bachelor's degree in a science or engineering field (or equivalent experience) * 2-4 years ...

New

CAI

Validation Engineer

Elkton, VA · On-site

$72K - $80K/yr

... Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Elkton, VA · On-site

$72K - $80K/yr

... Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Elkton, VA · On-site

$72K - $80K/yr

... Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Elkton, VA

$72K - $80K/yr

... Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Validation Engineer

Elkton, VA · On-site

$72K - $80K/yr

... Pharmaceutical facilities - Utilities - Equipment 3. Project & Team Management - Plan and ... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and ...

CAI

Senior Validation Engineer

Charlottesville, VA · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... the Pharmaceutical/Life Sciences industry - Essential experience in a GMP (Good Manufacturing ...

CAI

Senior Validation Engineer

Charlottesville, VA · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... the Pharmaceutical/Life Sciences industry - Essential experience in a GMP (Good Manufacturing ...

MSD

Senior Specialist, Engineering- Validation

Elkton, VA · On-site

$117K - $184K/yr

Minimum five (5) years of pharmaceutical manufacturing industry * Working in a cGMP environment ... CTU/WH qualification / validation; Dry Heat Depyrogenation qualification / validation; Steam ...

Merck & Co.

$117K - $184K/yr

Scheduling and executing PQ Validation activitiesScheduling and managing PQ protocol close ... Biochemistry, Biopharmaceutical Industry, Good Manufacturing Practices (GMP), Pharmaceutical ...

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All JobsPharmaceutical Validation Engineer JobsPharmaceutical Validation Engineer Jobs in Virginia

Pharmaceutical Validation Engineer information

See Virginia salary details

$22

$51

$77

How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for pharmaceutical validation engineer 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 does a pharmaceutical validation engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation engineer?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What are the most common challenges a pharmaceutical validation engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.

What is the difference between Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

What are popular job titles related to Pharmaceutical Validation Engineer jobs in Virginia?

For Pharmaceutical Validation Engineer jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Validation Engineer jobs in Virginia look for?

The top searched job categories for Pharmaceutical Validation Engineer jobs in Virginia are:

Pharmaceutical Validation Engineer jobs near you
Infographic showing various Pharmaceutical Validation Engineer job openings in Virginia as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $107,225 per year, or $51.6 per hour.

Validation Engineer

Doist

Elkton, VA • On-site

$85 - $110/hr

Other

Posted 3 days ago

New

Job description

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission‑critical and regulated industries needing to deliver essential solutions in high‑stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard—through our rigorous approach, field‑tested processes, and elite expertise developed over 30 years.

Our Purpose

We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.

Foundational Principles
  • We act with integrity
  • We serve each other
  • We serve society
  • We work for our future
  • We are relentless in our dedication to excellence, pushing boundaries and redefining industry standards.
Key ResponsibilitiesTechnical Responsibilities
  • Develop documentation for CQV activities
  • Write and execute protocols (field verification)
  • Develop summary reports at client sites
Areas of Focus
  • Pharmaceutical facilities
  • Utilities
  • Equipment
Project & Team Management
  • Plan and coordinate work
  • Direct small teams in document development and/or execution
Qualifications and Experience
  • Bachelor’s degree in a science or engineering field (or equivalent experience)
  • 2–4 years’ experience in commissioning and qualification in a regulated industry
  • Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus
  • Preferred experience in:
    • Facilities and equipment startup
    • Walk‑downs and troubleshooting
    • Utilities (WFI, RO, HVAC)
    • Upstream/downstream processing
    • Purification, recovery
    • Building automation
    • Pharmaceutical manufacturing processes
Influence Strategy
  • Pursues initiatives aligned with organizational strategy
  • Identifies strategic, innovative solutions
  • Anticipates emerging customer/market needs
Satisfy the Customer
  • Understands and anticipates customer needs
  • Delivers high‑quality solutions and service
  • Proactively maintains satisfaction and loyalty
Plan for Success
  • Aligns business strategies with actionable plans
  • Anticipates risks and builds contingency plans
  • Secures resources for goal achievement
Pursue Execution
  • Prioritizes time and resources effectively
  • Holds self and others accountable
  • Acts to overcome obstacles and improve quality
Tailor Communication
  • Communicates clearly and professionally
  • Adjusts style to fit the audience
  • Explains technical concepts effectively
Build Partnerships
  • Builds networks across functions
  • Encourages collaboration and breaks down silos
  • Involves stakeholders in decisions
Influence Others
  • Builds support with sound rationale
  • Gains buy‑in from decision makers
  • Encourages innovative thinking
Develop Self and Others
  • Enhances interpersonal relationships
  • Models integrity and company values
  • Seeks out growth and breakthrough opportunities

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