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Computer System Validation Manager Jobs in Ashburn, VA

Pinnaql

Digital Validation / QMS Specialist

Rockville, MD · On-site

$90 - $120/hr

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Experience with Validation Lifecycle Management Systems (VLMS) -- Veeva Validation Management ...

Guidehouse

Computer Systems Analyst

Rockville, MD · On-site

$98K - $163K/yr

The electronic chemical inventory system is the central critical component to this process, and the ... Knowledge of software license management, upgrades, patches, and compatibility validation.

Guidehouse

Computer Systems Analyst

Rockville, MD · On-site

$98K - $163K/yr

The electronic chemical inventory system is the central critical component to this process, and the ... Knowledge of software license management, upgrades, patches, and compatibility validation.

IT Excel

QA Tester

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Skills/Abilities/Competencies Required Required Interpersonal Skills Exceptional ...

IT Excel

QA Tester

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Skills/Abilities/Competencies Required Required Interpersonal Skills Exceptional ...

IT Excel

Business analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Minimum Experience: Recent college graduates with no experience or graduates with ...

IT Excel

Business analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Minimum Experience: Recent college graduates with no experience or graduates with ...

IT Excel

Entry Level QA Analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Qualifications Qualifications: BS in Biomedical Engineering/ BS in Chemical ...

IT Excel

Entry Level QA Analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Qualifications Qualifications: BS in Biomedical Engineering/ BS in Chemical ...

IT Excel

Entry Level QA Analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Minimum Experience: Recent college graduates with no experience or graduates with ...

IT Excel

Entry Level QA Analyst

Reston, VA · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Minimum Experience: Recent college graduates with no experience or graduates with ...

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Showing results 21-40

All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Ashburn, VA

Computer System Validation Manager information

See Ashburn, VA salary details

$48.6K

$107.8K

$164.1K

How much do computer system validation manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for computer system validation manager in Ashburn, VA is $107,798.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,200.00 and $135,000.00 per year, depending on experience, location, and employer.

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are the most commonly searched types of Computer System Validation jobs in Ashburn, VA?

The most popular types of Computer System Validation jobs in Ashburn, VA are:

What are popular job titles related to Computer System Validation Manager jobs in Ashburn, VA?

For Computer System Validation Manager jobs in Ashburn, VA, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Manager jobs in Ashburn, VA look for?

The top searched job categories for Computer System Validation Manager jobs in Ashburn, VA are:

Computer System Validation Manager jobs near you

Digital Validation / QMS Specialist

Pinnaql

Rockville, MD • On-site

$90 - $120/hr

Other

Posted 10 days ago

Job description

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Digital Validation / QMS Specialist
What you will do:
  • Facilitate and lead structured working sessions with cross-functional stakeholders (Validation, QC, Manufacturing, MSAT, Engineering) to define ~350 entities across Phase 1 and Phase 2.
  • Complete and route GVLMS worksheets within the Veeva Validation Management module, operating with Validation Lead role access within the Veeva Vault environment.
  • Pre-populate entity definition templates with available source data prior to each working session to maximize efficiency and minimize stakeholder time.
  • Ensure all GVLMS worksheets are completed, routed, and progressed through the approval workflow in compliance with 21 CFR Part 11 electronic record requirements.
  • Execute the scanning and Veeva upload of approximately 150 executed IOQ binders (estimated 50-200 pages each).
  • Follow the Document Control Room retrieval SOP for all binder access and chain-of-custody handling.
  • Build and maintain the Master Validation Data Repository — a traceability index covering 2-5 validation documents per system across ~350 qualified systems — drawing from documents already available in Veeva and the RMC Doc Control Room.
  • Verify upload accuracy against source binder index and elevate discrepancies within 1 business day.
Qualifications:
  • 3-5+ years of validation experience in a regulated pharmaceutical, biotech, or CDMO environment.
  • Direct hands-on experience authoring and revising GxP validation documents — VMPs, SOPs, Guidance Documents, and validation templates.
  • Experience with Validation Lifecycle Management Systems (VLMS) — Veeva Validation Management, Kneat, ValGenesis, or equivalent platform.
  • Familiarity with the Veeva Vault ecosystem, including document routing, approval workflows, and 21 CFR Part 11 electronic record management.
  • Experience executing IOQ binder documentation, scanning, and electronic document management in a GMP environment.
  • Demonstrated ability to facilitate cross-functional working sessions with quality, engineering, and manufacturing stakeholders.
Preferred Qualifications
  • Experience in a cell therapy, gene therapy, or advanced biologics GMP manufacturing environment.
  • Prior experience supporting a GVLMS implementation or digital validation platform rollout.
  • Direct experience with Veeva Validation Management — entity definition, worksheet creation, routing, and approval workflows.
  • Familiarity with SAP PM (Plant Maintenance) for calibration or requalification scheduling.
  • Experience supporting multiple concurrent document types under a single change control record.
  • Prior experience working on a Pinnaql or similar consulting/managed service engagement — you understand the accountability model.
  • Bachelor's degree in Life Sciences, Engineering, Chemistry, or a related field.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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