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Validation Manager Jobs in Virginia (NOW HIRING)

Phlow Corp.

Sr. Validation Manager

Petersburg, VA · On-site

Establish validation master plans (VMPs) and lifecycle validation programs. * Manage CQV budgets, schedules, and resource planning. Commissioning & Qualification * Oversee commissioning and ...

Phlow Corp

Sr. Validation Manager

Petersburg, VA · On-site

Establish validation master plans (VMPs) and lifecycle validation programs. * Manage CQV budgets, schedules, and resource planning. Commissioning & Qualification * Oversee commissioning and ...

Phlow Corp

Sr. Validation Manager

Petersburg, VA · On-site

Establish validation master plans (VMPs) and lifecycle validation programs. * Manage CQV budgets, schedules, and resource planning. Commissioning & Qualification * Oversee commissioning and ...

Civica Rx

Director, Validation

Petersburg, VA · On-site

... manage cleaning validation programs. Plan validation efforts using a risk-based approach. • ... Provide oversight and direction to Aseptic Processing Simulation (APS) and Air Visualization ...

Syner-G

Validation Engineer

Middletown, VA · On-site

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... We are seeking a hands-on Validation Engineer with a strong background in mechanical or ...

Civica Rx

Director, Validation

Petersburg, VA

... manage cleaning validation programs. Plan validation efforts using a risk-based approach. · ... Provide oversight and direction to Aseptic Processing Simulation (APS) and Air Visualization ...

Syner-G

Validation Engineer

Middletown, VA

Through our expertise, insight, consulting and management skills, we accelerate breakthrough ... We are seeking a hands-on Validation Engineer with a strong background in mechanical or ...

Lancesoft

Validation Engineer

Middletown, VA · On-site

$65/hr

The Validation Engineer will support execution of validation activities for the MDT Validation ... Ability to manage multiple tasks within a structured project timeline * Comfortable working onsite ...

Syner-G

Validation Engineer

Middletown, VA · On-site +1

The role also involves managing smaller projects and collaborating across teams to ensure ... Ensure validation programs meet GMP, FDA, and ISO standards. * Support design and execution of ...

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

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See Virginia salary details

$47.1K

$104.5K

$159.1K

How much do validation manager jobs pay per year?

As of May 31, 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.

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.

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 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.

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 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.

More about Validation Manager jobs
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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
Sr. Validation Manager

Sr. Validation Manager

Phlow Corp

Virginia State University, VA

Other

Posted 13 days ago

Job description

Description

Leadership & Strategy

  • Develop and implement site-wide CQV strategies aligned with regulatory and business objectives.
  • Cleaning validation
  • Stability programs
  • Packaging configurations for intermediate and finished goods.
  • Lead, mentor, and develop CQV engineers and validation specialists.
  • Establish validation master plans (VMPs) and lifecycle validation programs.
  • Manage CQV budgets, schedules, and resource planning.

Commissioning & Qualification

  • Oversee commissioning and qualification of:
  • Manufacturing equipment
  • Clean utilities (WFI, clean steam, compressed gases)
  • HVAC systems and cleanrooms
  • Laboratory systems
  • Process automation and control systems
  • Establish and implement cleaning validation requirements.
  • Establish and implement packaging configurations
  • Stability programs and protocols
  • Ensure execution of URS, FRS, DS, FAT, SAT, IQ, OQ, and PQ protocols.
  • Coordinate with Engineering, Quality, Manufacturing, and external vendors.

Validation Lifecycle Management

  • Ensure compliance with:
  • FDA 21 CFR Parts 210/211, 11
  • EU GMP Annex 1 & 15
  • ICH guidelines
  • ISPE Baseline Guides
  • Oversee process validation, cleaning validation, and continued process verification (CPV).
  • Support technology transfer and new product introductions (NPI).

Documentation & Compliance

  • Review and approve validation protocols and reports.
  • Ensure data integrity and adherence to ALCOA+ principles.
  • Support internal audits, regulatory inspections, and client audits.
  • Manage deviation investigations, CAPAs, and change controls related to CQV.

Risk Management

  • Apply risk-based validation approaches (ICH Q9).
  • Conduct and facilitate FMEAs and risk assessments.
  • Implement continuous improvement initiatives in validation processes.

Requirements

Education

  • Bachelor's degree in Engineering, Pharmaceutical Sciences, or related technical field (Master's preferred).

Experience

  • 8+ years of experience in pharmaceutical/biotech manufacturing.
  • 5+ years in CQV/validation leadership role.
  • Strong knowledge of GMP-regulated environments.
  • Experience supporting regulatory inspections.

Technical Skills

  • Deep understanding of validation lifecycle approach.
  • Expertise in cleanroom and sterile manufacturing qualification (preferred).
  • Knowledge of automation systems (DeltaV, Siemens, etc.).
  • Familiarity with Kneat, ValGenesis, TrackWise, or similar systems (preferred).

Soft Skills

  • Strong leadership and team management skills.
  • Excellent communication and stakeholder engagement abilities.
  • High attention to detail and organizational skills.
  • Ability to manage multiple complex projects simultaneously.

Key Competencies

  • Regulatory Compliance Expertise
  • Project Management
  • Risk-Based Thinking
  • Cross-Functional Collaboration
  • Problem Solving & Decision Making
  • Continuous Improvement

Preferred Certifications:

  • PMP (Project Management Professional)
  • ASQ Certified Quality Engineer (CQE)
  • ISPE membership or relate industry certifications

Physical Requirements

  • Majority of time spent in a manufacturing environment with potential exposure to chemicals and controlled substances.
  • Must be able to wear appropriate PPE and occasionally lift up to 30 pounds.
  • May be required to be on call or work off-hours to support 24/7 operations.

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