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Pharma Validation Engineer Jobs (NOW HIRING)

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 ...

Sebela Pharma

CQV/Validation Engineer

Holbrook, MA · On-site

$33 - $43/hr

The CQV/Validation Engineer is responsible for supporting the activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations.

PCI Pharma Services

VALIDATION ENGINEER IV

Bedford, NH · On-site

The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

PCI Pharma Services

VALIDATION ENGINEER IV

Bedford, NH · On-site

The Validation Engineer IV performs an array of well-defined validation activities in support of ... PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully ...

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Pharma Validation Engineer information

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$78

How much do pharma validation engineer jobs pay per hour?

As of Aug 16, 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 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.

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.

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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 38% Full Time, and 62% Contract. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.

Test Method Validation (TMV) SME

Stark Pharma Solutions Inc

Newark, DE • Remote

Contractor

Re-posted 10 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Test Method Validation SME position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Test Method Validation (TMV) SME

Duration: 6–9 Month Contract (Extension Possible)
Experience: 10+ Years

Job Overview

We are seeking experienced Test Method Validation (TMV) Subject Matter Experts to lead and support TMV execution activities for complex medical device validation projects. This is a senior-level role requiring extensive experience in test method validation, technical leadership, and mentoring validation teams. Candidates should have a strong background in software and hardware validation within regulated environments.

Key Responsibilities

  • Lead and oversee TMV test execution activities for medical device validation projects.
  • Provide technical guidance and mentorship to validation engineers during protocol execution.
  • Review and support the development of TMV protocols, test methods, and acceptance criteria.
  • Ensure validation activities comply with design controls, quality standards, and regulatory requirements.
  • Monitor software and hardware validation testing, resolve execution issues, and ensure accurate documentation.
  • Collaborate with cross-functional engineering and quality teams to support successful project execution.

Required Qualifications

  • Bachelor's degree in Engineering or a related technical discipline.
  • 10+ years of U.S. experience as a TMV Lead, SME, Coach, or Validation Supervisor.
  • Hands-on experience executing Test Method Validation (TMV) test cases.
  • Strong background in software and hardware validation within the medical device industry.
  • Excellent leadership, mentoring, and technical problem-solving skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com