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Validation Jobs in Maryland (NOW HIRING)

Stark Pharma Solutions Inc

MD · On-site

I am working on Validation Engineer right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed is as follows Position: Validation ...

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, 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 ...

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How much do validation jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for validation in Maryland is $50.46, according to ZipRecruiter salary data. Most workers in this role earn between $38.27 and $61.35 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 Maryland?

The most popular types of Validation jobs in Maryland are:

What cities in Maryland are hiring for Validation jobs?

Cities in Maryland with the most Validation job openings:

Validation jobs near you
Infographic showing various Validation job openings in Maryland as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $104,966 per year, or $50.5 per hour.

Validation Engineer / Validation Specialist

Stark Pharma Solutions Inc

MD • On-site

Contractor

Re-posted 12 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Validation Engineer right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Validation Engineer / Validation Specialist

Location: Maryland
Duration: Long-Term Contract

Job Overview

We are seeking an experienced Validation Engineer/Validation Specialist to support equipment, utilities, and facility qualification activities in a GMP-regulated pharmaceutical/biotechnology manufacturing environment. The ideal candidate will have hands-on experience executing validation protocols and supporting commissioning, qualification, and compliance initiatives.

Key Responsibilities

  • Develop, execute, and document IQ, OQ, PQ, and Requalification (RQ) protocols for manufacturing equipment and utilities.
  • Prepare validation reports, SOPs, risk assessments, gap analyses, and technical documentation following GDP and cGMP requirements.
  • Perform thermal mapping studies using Kaye AVS or Veriteq data loggers.
  • Analyze validation data and investigate deviations to ensure compliance with acceptance criteria.
  • Support commissioning, FAT/SAT, equipment startup, and qualification activities.
  • Assist with audits and provide technical support for manufacturing and validation investigations.
  • Review validation documentation and collaborate with Engineering, Manufacturing, Quality, and Maintenance teams.

Required Qualifications

  • Bachelor's degree in Engineering or a related scientific discipline with 4+ years of validation experience, or 8+ years of relevant validation experience without a degree.
  • Hands-on experience in GMP pharmaceutical or biotechnology manufacturing.
  • Strong knowledge of IQ/OQ/PQ, cGMP, GDP, and validation lifecycle.
  • Experience with aseptic processing, cleanrooms, sterilization equipment, and critical utilities (HVAC, WFI, RO, compressed air, etc.).
  • Familiarity with Kaye AVS, Veriteq, EDMS, LIMS, Microsoft Office, and related validation systems.
  • Excellent troubleshooting, documentation, and communication skills.
  • Ability to manage multiple projects independently and in a team environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com