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Pharma Validation Jobs (NOW HIRING)

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 ...

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 ...

EQVAL Group, Inc

Validation Engineer

Ponce, PR · On-site

Minimum of 4+ years of experience in Pharma, Biotech, or Medical Devices. * Experienced in development and execution of validation documentation and protocols, including; Validation Assessments ...

PCI Pharma Services

Validation Analyst 3

Rockford, IL · On-site

$27.27 - $30.68/hr

The Validation Analyst III is responsible for overall validation project management of large ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

PCI Pharma Services

Validation Analyst 3

Rockford, IL

$27.27 - $30.68/hr

The Validation Analyst III is responsible for overall validation project management of large ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

BioPhase Solutions

Validation Engineer

Los Angeles, CA · On-site

$115K/yr

Certifications related to GMP compliance, quality systems, or validation preferred. * 1-3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

The role focuses on implementing best practices, supporting site and process improvement projects, and maintaining GMP-compliant validation and quality systems within a regulated Biotech/Pharma ...

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Pharma Validation information

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$22

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How much do pharma validation jobs pay per hour?

As of Jun 12, 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.
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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 100% Full Time. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Validation Engineer

Validation Engineer

Intellectt INC

New York, NY • On-site

Contractor

Posted 23 days ago

Job description

Hello,
I Hope you are doing great.

This is Mahaboob from Intellectt INC; We have an urgent opening for a Validation Engineer position based in New York with one of our prestigious clients.
If you are interested or know someone who might be a good fit, please share your updated resume at mahaboob.m@intellectt.com.
Job Title: Validation Engineer
Location: New York
Summary:
Seeking a Validation Engineer with strong experience in analytical instruments and CSA/CSV to support GMP operations in biologics / cell & gene therapy environments.
Key Responsibilities:

  • Execute IQ/OQ/PQ for HPLC, GC, LC-MS, UV, dissolution systems
  • Perform CSA/CSV for lab systems (LIMS, Empower, Chromeleon)
  • Develop validation docs: URS, risk assessments, protocols, reports
  • Ensure compliance with 21 CFR Part 11, GAMP 5, Data Integrity (ALCOA+)
  • 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 & gene therapy preferred

Thanks & Regards,
Mahaboob M
Technical Recruiter
Intellectt Inc 
mahaboob.m@intellectt.com
Direct: 732-276-1830
Desk number: 732 412 6999- Ext: 355