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Validation Engineer Iii Jobs (NOW HIRING)

JSat Automation

Validation Engineer

Glendale, CA · On-site

The Validation Engineer will be responsible for the following. * Develop, approve, and execute ... Chemical engineers preferred, with a minimum of three (3) years relevant experience. * Experience ...

Intellectt INC

Validation Engineer

Boston, MA · On-site

Validation Engineer Location: Boston, MA Overview This engagement supports a large-scale Quality ... Support audit readiness and inspection activities Qualifications * 3-5 years experience in ...

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

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 ...

Sigan America LLC

Validation Engineer

Ottawa, IL · On-site

$90K - $100K/yr

Bachelor's degree in Engineering, Life Sciences, or a related technical field (or equivalent experience). * 3-5+ years of validation experience in a pharmaceutical, medical device, cosmetic, or other ...

Blue Bird

Validation Engineer

Fort Valley, GA

JOB SUMMARY The Validation Engineer in Engineering designs develops, and executes physical ... Minimum of 3 to 5 years of experience in experimental validation, laboratory testing, or physical ...

Catalyx

Validation Engineer

Horsham, PA

Catalyx Services, LLC seeks a Validation Engineer reporting to office in Montgomeryville, PA to ... three (3) years of experience as an Automation Engineer or a substantially similar position ...

Blue Bird

Validation Engineer

Fort Valley, GA · On-site

JOB SUMMARY The Validation Engineer in Engineering designs develops, and executes physical ... Minimum of 3 to 5 years of experience in experimental validation, laboratory testing, or physical ...

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Validation Engineer Iii information

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How much do validation engineer iii jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for validation engineer iii 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 the difference between Validation Engineer Iii vs Validation Engineer Ii?

AspectValidation Engineer IiiValidation Engineer Ii
Required CertificationsGMP, GxP, or industry-specific validation certificationsGMP, GxP, or industry-specific validation certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingPharmaceutical, biotech, or medical device manufacturing
Experience LevelAdvanced, with 3+ years of validation experienceIntermediate, with 1-3 years of validation experience
Job ResponsibilitiesLeading validation projects, complex troubleshooting, mentoringSupporting validation activities, executing protocols

The Validation Engineer Iii typically has more experience and handles complex validation projects, often leading initiatives and mentoring junior staff. In contrast, Validation Engineer Ii focuses on supporting validation tasks and executing protocols under supervision. Both roles are common in regulated industries like pharmaceuticals and biotech, with the Iii level requiring more expertise and responsibility.

What skills and qualifications are needed to thrive as a Validation Engineer III?

To excel as a Validation Engineer III, you need a strong background in engineering or life sciences, extensive knowledge of validation protocols, and experience in regulated industries such as pharmaceuticals or medical devices. Familiarity with technical tools like validation lifecycle management software, statistical analysis packages, and regulatory standards (e.g., FDA, GMP) is typically required, along with relevant certifications such as Six Sigma or CQE. Critical thinking, attention to detail, and effective communication are crucial soft skills for documenting processes and collaborating with cross-functional teams. These competencies ensure compliance, product quality, and the successful execution of complex validation projects.

What are the roles and responsibilities of a Validation Engineer III?

A Validation Engineer III is responsible for ensuring that products, processes, and systems meet regulatory and company standards for quality and safety. This role typically involves planning and executing validation tests, writing protocols and reports, analyzing data, and troubleshooting validation issues. Validation Engineer IIIs often lead validation projects, mentor junior staff, and work closely with cross-functional teams in industries like pharmaceuticals, biotechnology, or manufacturing. They ensure compliance with regulatory requirements such as FDA, GMP, or ISO standards. Strong analytical, documentation, and project management skills are important for success in this position.

What are common challenges faced by a Validation Engineer III, and how can they be addressed?

As a Validation Engineer III, one common challenge is coordinating among cross-functional teams such as manufacturing, quality, and regulatory departments to ensure validation activities meet strict compliance standards and timelines. Managing multiple projects simultaneously while adhering to evolving regulatory requirements can also be demanding. Strong project management, effective communication, and staying updated on industry guidelines help address these challenges and ensure successful validation outcomes.
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What states have the most Validation Engineer Iii jobs? States with the most job openings for Validation Engineer Iii jobs include:
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Validation Engineer Iii jobs near you
Infographic showing various Validation Engineer Iii job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Engineer III, Validation - Process & Cleaning

Thermo Fisher Scientific

Greenville, NC

Full-time

Re-posted 2 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 537 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

Job Description

Discover Impactful Work:

Join Thermo Fisher Scientific and be part of a team delivering life-changing therapies through world-class sterile pharmaceutical manufacturing.

As a Validation Engineer III, you will lead validation activities supporting process and cleaning validation in sterile environments, playing a key role in ensuring compliance, quality, and successful product launches.

This role offers high visibility and cross-functional exposure, working across Operations, Quality, and QC Labs—often acting as a technical lead during tech transfers and validation execution.

A Day in the Life:
  • ~70% desk-based: protocol writing, data analysis, deviation investigations, reporting
  • ~30% on the floor: executing validation in sterile manufacturing environments
  • Lead validation activities including:
    • Process validation
    • Cleaning validation
    • Equipment qualification (IQ/OQ/PQ)
  • Support tech transfers and new product introductions
  • Collaborate cross-functionally with Ops, QC, and Quality teams
  • Participate in client interactions, audits, and regulatory readiness
What to Expect:
  • Ownership of complex validation projects
  • High exposure across site operations and leadership teams
  • Opportunity to act in a project management capacity
  • Involvement in audits, deviations, and continuous improvement
Keys to Success:Education & Experience:
  • Bachelor’s degree and 4+ years validation experience
  • Experience in pharmaceutical or biotech manufacturing required
  • Direct experience in sterile/aseptic pharmaceutical manufacturing highly preferred:
    • Aseptic filling
    • Sterile processing
    • Cleanroom environments
Skills & Expertise:
  • Strong experience with:
    • Process validation
    • Cleaning validation
    • Equipment qualification (IQ/OQ/PQ)
  • Proven ability to write and execute validation protocols and reports
  • Experience with validation documentation and regulatory standards
  • Exposure to audits, audit responses, or regulatory inspections
  • Strong problem-solving and deviation investigation skills
Preferred:
  • Experience in both process and cleaning validation
  • Background in sterile filling or manufacturing operations
  • Knowledge of FDA, EMA, and cGMP regulations
Work Environment & Requirements:
  • Onsite role in Greenville, NC
  • Monday–Friday schedule with flexibility as needed
  • Cleanroom and production floor exposure required
Why Join Us:
  • Work on cutting-edge sterile pharmaceutical programs
  • Gain broad cross-functional exposure across the site
  • Be part of high-impact tech transfers and product launches
  • Clear path to senior and leadership roles

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