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Validation Manager Jobs in Frederick, MD (NOW HIRING)

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

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

Valid NPI. * CAQH validation/re-validation. * Registered in ePrep. * Current commercial liability insurance. Experience: * At least one (1) year providing Case Management. * At least one (1) year in ...

Summary: The Technical Manager will oversee a laboratory team providing technical expertise ... Support development and validation of research assays. * Coordinate with scientific and ...

Technical Manager

Fort Detrick, MD · On-site

$80K - $90K/yr

Summary: The Technical Manager will oversee a laboratory team providing technical expertise ... Support development and validation of research assays. * Coordinate with scientific and ...

This Project Management Assistant position provides support to Project Managers who oversee ... Gather, organize and validate data for project financial forecasts * Input data into various ...

This Project Management Assistant position provides support to Project Managers who oversee ... Gather, organize and validate data for project financial forecasts * Input data into various ...

This Project Management Assistant position provides support to Project Managers who oversee ... Gather, organize and validate data for project financial forecasts * Input data into various ...

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Validation Manager information

See Frederick, MD salary details

$47.2K

$104.8K

$159.6K

How much do validation manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for validation manager in Frederick, MD is $104,811.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,100.00 and $131,200.00 per year, depending on experience, location, and employer.

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 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.

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.

What are the most commonly searched types of Validation jobs in Frederick, MD? The most popular types of Validation jobs in Frederick, MD are:
What job categories do people searching Validation Manager jobs in Frederick, MD look for? The top searched job categories for Validation Manager jobs in Frederick, MD are:
What cities near Frederick, MD are hiring for Validation Manager jobs? Cities near Frederick, MD with the most Validation Manager job openings:
Infographic showing various Validation Manager job openings in Frederick, MD as of July 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $104,811 per year, or $50.4 per hour.

Validation Engineer - Equipment & Utilities

Apetan Consulting llc

Frederick, MD • On-site

$80 - $150/hr

Contractor

Posted 23 days ago


Job description

Title: Equipment & Utility Validation Engineer / Specialist

Location: Frederick, Maryland (Onsite) – Need Local or Nearby non-local accepted who can relocate at their own cost.

Duration: 6+ months

Job Overview:
We are seeking highly experienced Equipment & Utility Validation Engineers/Specialists to support pharmaceutical and biotech manufacturing operations in a GMP-regulated environment. The ideal candidate will have strong expertise in commissioning, qualification, validation (CQV), and utility systems validation with hands-on experience in FDA-regulated facilities.

Key Responsibilities:

  • Execute equipment and utility qualification activities including IQ, OQ, and PQ
  • Develop, review, and execute validation protocols and reports
  • Perform commissioning and qualification (CQV) activities for manufacturing and utility systems
  • Validate clean utilities including WFI, RO, Clean Steam, HVAC, and compressed gases
  • Support deviation investigations, CAPA, change controls, and risk assessments
  • Ensure compliance with GMP, FDA, ISPE, and regulatory standards
  • Collaborate with Engineering, QA, Manufacturing, and Validation teams
  • Maintain accurate validation and compliance documentation

Required Skills:

  • Strong experience with Equipment & Utility Validation in Pharma/Biotech environments
  • Hands-on expertise with IQ/OQ/PQ and CQV processes
  • Knowledge of GMP/GxP compliance requirements
  • Experience with utility systems validation and process equipment qualification
  • Excellent documentation and communication skills
  • Ability to work independently in fast-paced regulated environments

Preferred:

  • Experience supporting FDA audits and inspections
  • Familiarity with Kneat, ValGenesis, or other validation management tools
  • Strong troubleshooting and analytical skills