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Validation Jobs in Frederick, MD (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 ...

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All JobsValidation JobsValidation Jobs in Frederick, MD

Validation information

See Frederick, MD salary details

$22

$51

$77

How much do validation jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for validation in Frederick, MD is $51.70, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $62.84 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 Frederick, MD?

The most popular types of Validation jobs in Frederick, MD are:

What cities near Frederick, MD are hiring for Validation jobs?

Cities near Frederick, MD with the most Validation job openings:

Validation jobs near you
Infographic showing various Validation job openings in Frederick, MD as of August 2026, with employment types broken down into 85% Full Time, 11% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $107,533 per year, or $51.7 per hour.

Validation Engineer / Validation Specialist

Stark Pharma Solutions Inc

Frederick, MD • On-site

Contractor

Posted 18 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 validation activities within a GMP manufacturing facility. The successful candidate will be responsible for preparing and executing qualification protocols, generating validation documentation, supporting equipment and utility validation, and ensuring compliance with cGMP and Good Documentation Practices.

Key Responsibilities

  • Prepare and execute IQ/OQ/PQ/RQ protocols and reports for new and existing equipment and utilities.
  • Develop acceptance criteria based on industry standards, manufacturer recommendations, user/functional specifications, and current cGMP requirements.
  • Generate validation summary reports in accordance with Good Documentation Practices (GDP).
  • Perform thermal mapping studies using Kaye AVS or Veriteq dataloggers.
  • Develop and revise Standard Operating Procedures (SOPs).
  • Analyze validation data and verify compliance with established acceptance criteria.
  • Document and support resolution of deviations associated with qualification activities.
  • Assist with Commissioning, FAT, and SAT activities as required.
  • Prepare technical documentation including validation reports, gap assessments, and risk assessments.
  • Provide technical and investigative support for troubleshooting and resolving manufacturing equipment issues.
  • Perform technical reviews of qualification and validation documents prepared by other team members.
  • Support facility and validation activities related to regulatory and client audits.

Required Qualifications

  • Bachelor's degree in Engineering, Science, or a related field.
  • Minimum 4 years of applicable validation experience with a bachelor's degree, or 8 years of applicable experience in lieu of a bachelor's degree.
  • Hands-on validation experience in GMP biotechnology or pharmaceutical manufacturing environments.
  • Experience with IQ/OQ/PQ/RQ qualification activities.
  • Strong working knowledge of cGMP and Good Documentation Practices.
  • Experience and knowledge of aseptic processing.
  • Hands-on experience with sterilization equipment, cleanroom environments, cleaning processes, and critical utilities such as HVAC, WFI, RO, and CCA.
  • Knowledge of computerized control systems and isolator technology.
  • Experience using Microsoft Office and electronic systems such as EDMS, RAM, and LIMS.
  • Strong written and verbal communication skills with excellent attention to detail.
  • Ability to manage multiple projects and work effectively both independently and as part of a team.
  • General knowledge of maintenance and calibration procedures is desirable.