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Pharma Validation Jobs (NOW HIRING)

Intellectt INC

Validation Engineer II

Bothell, WA · On-site

We are looking for a CQV / Validation Engineer with 5-8 years of experience in GMP-regulated pharma/biotech environments. This role focuses on executing equipment qualification and supporting ...

Motion Recruitment

Validation Engineer

Oro Valley, AZ · On-site

$39 - $42/hr

We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and ...

Aequor

Specialist QA - Validation, cGMP

Woburn, MA

Company Description Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs ...

Intellectt INC

Validation Engineer

New York, NY · On-site

Support method validation, change control, and audits Requirements: * 4-6+ years in GMP validation (pharma/biotech) * Hands-on with analytical instruments + CSA/CSV * Experience in biologics / cell ...

Adare Pharma

Validation Engineer

Vandalia, OH · On-site

Our Business Adare Pharma Solutions is a global Contract Development and Manufacturing Organization ... Position Validation Engineer Location Vandalia, Ohio Summary In this position, the Engineer will ...

Catalent Pharma Solutions

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or ... a valid written & signed search agreement, will become the sole property of Catalent. No fee will ...

Tekhawks LLC

Be Seen First

Validation Engineer - (Medical Device, Pharma)

Jacksonville, FL · On-site

$35 - $40/hr

Validation Engineer Location: Jackson, FL Duration: 1.5-year contract Hours per week: 40+ We are seeking two mid-level Validation Engineers to support a large capital expansion at a leading medical ...

Tekhawks LLC

Be Seen First

Validation Engineer - (Medical Device, Pharma)

Jacksonville, FL · On-site

$35 - $40/hr

Validation Engineer Location: Jackson, FL Duration: 1.5-year contract Hours per week: 40+ We are seeking two mid-level Validation Engineers to support a large capital expansion at a leading medical ...

JSat Automation

Validation Engineer

Glendale, CA · On-site

JSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. * Develop, approve, and execute process ...

Catalent, Inc.

Validation Specialist

Winchester, KY · On-site

Validation Specialist Position Summary * Typical working hours are Monday-Friday 8 AM-5 PM * This ... Other duties as required in support of Catalent Pharma Solutions high performance The Candidate

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All JobsPharma Validation Jobs

Pharma Validation information

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$22

$51

$78

How much do pharma validation jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for pharma validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is pharma validation?

Pharma validation is the process of ensuring that pharmaceutical manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards and regulatory requirements. This process involves documenting and verifying each step in the manufacturing process to ensure safety, efficacy, and compliance. Validation activities include installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Proper validation helps minimize risks, ensures patient safety, and is a critical requirement for regulatory approval by agencies like the FDA.

What are the key skills and qualifications needed to thrive in Pharma Validation, and why are they important?

To thrive in Pharma Validation, you need a strong background in pharmaceutical sciences, regulatory compliance, and validation protocols, often supported by a relevant degree such as pharmacy, chemistry, or engineering. Familiarity with validation tools, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring thorough documentation and collaboration with cross-functional teams. These skills ensure all processes and products meet stringent regulatory standards, safeguarding product quality and patient safety.

What is the difference between Pharma Validation vs Quality Assurance Specialist?

AspectPharma ValidationQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality departments, production sites
Industry UsageEnsures equipment, processes meet standardsMaintains quality systems, audits

Pharma Validation focuses on verifying that equipment, processes, and systems meet regulatory standards through validation protocols. Quality Assurance Specialists oversee overall quality systems, conduct audits, and ensure compliance. While both roles aim to ensure product quality, Validation is more technical and process-specific, whereas QA Specialists handle broader quality management and compliance activities.

What are some typical challenges faced by professionals in pharma validation, and how can they be addressed?

Pharma validation professionals often encounter challenges such as keeping up with ever-evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation throughout the validation process. Addressing these challenges requires ongoing training on current Good Manufacturing Practices (cGMP), effective project management skills, and close collaboration with cross-functional teams such as quality assurance and production. Proactively communicating with stakeholders and staying organized can help mitigate risks and ensure compliance.
More about Pharma Validation jobs
What states have the most Pharma Validation jobs? States with the most job openings for Pharma Validation jobs include:
What job categories do people searching Pharma Validation jobs look for? The top searched job categories for Pharma Validation jobs are:
Pharma Validation jobs near you
Infographic showing various Pharma Validation job openings in the United States as of June 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Validation Engineer II

Validation Engineer II

Intellectt INC

Bothell, WA • On-site

Contractor

Posted 6 days ago

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Validation Engineer II based in Bothell, WA  with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com
Job Title: Validation Engineer II (Onsite)
Location: Bothell, WA 

Overview:
We are looking for a CQV / Validation Engineer with 5–8 years of experience in GMP-regulated pharma/biotech environments. This role focuses on executing equipment qualification and supporting validation activities across systems and processes.

Key Responsibilities:

  • Execute equipment qualification (IQ/OQ/PQ)
  • Support commissioning and qualification (CQV) activities
  • Author and execute validation protocols and reports
  • Assist in process validation (PPQ)
  • Collaborate with engineering, manufacturing, and quality teams
  • Support deviations, CAPAs, and change control activities
  • Ensure compliance with GMP standards

Requirements:

  • 5–8 years of CQV/Validation experience in pharma/biotech
  • Strong hands-on experience with IQ/OQ/PQ
  • Experience in GMP-regulated environments
  • Skilled in validation documentation and execution
  • Ability to work cross-functionally in onsite settings

Nice to Have:

  • Cleaning validation experience
  • Exposure to PPQ
  • Utilities/facility qualification experience
  • Experience in biologics or drug substance manufacturing

    Thanks & Regards,
    Vyshnavi
    Recruiter
    Intellectt Inc 
    Vyshnavi.t@intellectt.com
    Direct: 732 204 6550
    Desk number: 732 412 6999- Ext: 225