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Pharma Validation Engineer Jobs (NOW HIRING)

Kite Pharma

Sr Validation Engineer I

Oceanside, CA

We are seeking a highly effective Senior Validation Engineer responsible for planning, execution ... Master's degree with 5+yearsof experience in validation in a biotech/pharma industry * Experience ...

Frontwell Solutions

$110 - $150/hr

You will play a pivotal role in modernizing quality management systems, implementing Pharma 4.0 ... Implement and support paperless validation solutions (e.g., Kneat, Valgenesis, Polarion, DevOps, ...

New

System One

QA Validation Engineer

Bethlehem, PA · On-site

Job Title: QA Validation Engineer Location: Bethlehem, PA Type: Direct Hire Compensation: $95-110k ... Must come from a regulated environment - food, pharma, chemical * Must have experience working with ...

System One

QA Validation Engineer

Bethlehem, PA · On-site

Job Title: QA Validation Engineer Location: Bethlehem, PA Type: Direct Hire Compensation: $95-110k ... Must come from a regulated environment - food, pharma, chemical * Must have experience working with ...

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How much do pharma validation engineer jobs pay per hour?

As of Sep 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 is a pharma validation engineer?

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.

What does a pharma validation engineer do?

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 skills and qualifications are needed to be a pharma validation engineer?

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.

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Pharma Validation Engineer jobs near you
Infographic showing various Pharma Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant

Two River Consulting Partners

Summit, NJ • On-site

$80 - $100/hr

Other

Re-posted 6 days ago

Job description

0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant

Please contact Amanda Mazza: amanda@tworivercp.com

Job Overview

We are seeking an experienced CSV Engineer to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The ideal candidate should have hands‑on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.

Validation Engineer Responsibilities
  • Support CSV activities for ELLA and Synergy Neo2 instrument implementation
  • Develop, review, and/or execute validation deliverables including validation plans, risk assessments, test protocols, traceability matrices, summary reports, and related documentation
  • Partner with laboratory, Quality, IT, and project stakeholders to ensure validation activities are completed on schedule
  • Support GxP compliance, data integrity, and 21 CFR Part 11 considerations as applicable
  • Manage validation workstreams for both instruments simultaneously
  • Identify and escalate risks, gaps, delays, or documentation issues
  • Support deviation resolution and documentation updates during protocol execution
Job Requirements
  • Strong CSV experience in a GxP laboratory or regulated life sciences environment
  • Prior experience with laboratory instrument implementation and validation
  • Experience with ELLA and Synergy Neo2 strongly preferred
  • Ability to manage multiple validation activities or technologies concurrently
  • Familiarity with IQ/OQ/PQ, CSV lifecycle documentation, risk‑based validation, data integrity, and Part 11 expectations
  • Strong communication skills and ability to work effectively with cross‑functional teams
  • Experience supporting ECQ or lab equipment qualification
  • Experience in biotech, pharma, plasma, or manufacturing laboratory environments
  • Prior experience working in client‑facing hybrid/onsite roles

This role can be a local/hybrid setup. At minimum, a 50% on‑site presence is required.

LOCATION

50% onsite in Summit, NJ

EMPLOYMENT

Competitive C2C or W2 Contractor

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