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Pharma Validation Engineer Jobs (NOW HIRING)

Intellectt INC

Validation Engineer

New York, NY · On-site

We have an urgent opening for a Validation Engineer position based in New York with one of our ... years in GMP validation (pharma/biotech) * Hands-on with analytical instruments + CSA/CSV

Peregrine Team

Validation Engineer

Philadelphia, PA · On-site

Bachelor's degree in Engineering or related field * 3-5+ years of validation experience in pharma/biotech * Knowledge of cGMP and validation standards * Strong documentation and technical skills

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 ...

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 ...

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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 ...

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 ...

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Pharma Validation Engineer information

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How much do pharma validation engineer jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for pharma validation engineer 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 does a typical day look like for a Pharma Validation Engineer?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

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

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

What is a Pharma Validation Engineer job?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

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Pharma Validation Engineer jobs near you

Validation Engineer (CQV, GMP, Life Sciences)

VBB

Chicago, IL • On-site

$70K - $100K/yr

Full-time

Posted 12 days ago

Job description

Validation Engineer (CQV, GMP, Life Sciences)
  • Location: Greater Chicago
  • Salary: $70-100K + Bonus + Benefits
  • No Sponsorship, No Relocation

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We're hiring a Validation Engineer who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.
What You'll Do
  • Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
  • Work on validation of lab systems, equipment, and utilities
  • Partner with engineering, validation teams, and lab stakeholders
  • Assist with project scheduling, coordination, and resource planning
  • Support commissioning & qualification (CQV) activities across projects
  • Contribute to GMP / GxP documentation and compliance efforts
  • Learn to lead validation workstreams and progress into a Validation Project Lead role
What We're Looking For
  • 5+ years of experience in:
    • Validation Engineering
    • CQV (Commissioning, Qualification, Validation)
    • or GMP-regulated environments (Pharma / Biotech)
  • Strong understanding of:
    • GMP / GxP / FDA regulations
    • Validation lifecycle (IQ/OQ/PQ)
  • Ability to work cross-functionally with engineering, QA, and operations teams
  • Strong communication and problem-solving skills
  • Coachable, driven, and motivated to grow into leadership
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally (project-based work)
  • Experience with validation documentation, protocols, and execution
Nice to Have
  • Experience with lab systems, utilities, or manufacturing equipment validation
  • Exposure to commissioning activities (C&Q / CQV)
  • Familiarity with AI tools for validation or documentation
Why This Role
  • Hands-on experience across pharma validation projects
  • Clear path into senior validation or project leadership roles
  • Work alongside experienced engineers in regulated environments

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer
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