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Contract Validation Engineer Jobs (NOW HIRING)

adareps

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 ...

Intellectt INC

Process Validation Engineer

Manchester, NH · On-site

My name is Mahalakshmi, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Process Validation Engineer based in Manchester, NH with one of our prestigious ...

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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 ...

Cynet Systems

Validation Engineer 1 Job Location: Markham, ON Job Type ... Contract Job Overview: Requirement/Must Have: * In-depth knowledge of SoC architecture, computer ...

Intellectt INC

Mold Validation Engineer

Minneapolis, MN · On-site

My name is Bipasa , and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Mold Validation Engineer based in Minneapolis, MN with one of our prestigious clients. I ...

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Cynet Systems

Validation Engineer 2 Job Location: Markham, ON Job Type ... Contract Job Overview: Requirement/Must Have: * In-depth knowledge of SoC architecture, computer ...

Intellectt INC

Process Validation Engineer

Manchester, NH · On-site

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Process Validation Engineer based in Manchester, NH with one of our prestigious clients. I ...

Apply Early

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Contract Validation Engineer information

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$22

$51

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How much do contract validation engineer jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for contract 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 are the primary responsibilities of a Contract Validation Engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

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

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

What is a Contract Validation Engineer job?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

More about Contract Validation Engineer jobs
What cities are hiring for Contract Validation Engineer jobs? Cities with the most Contract Validation Engineer job openings:
What are the most commonly searched types of Validation Engineer jobs? The most popular types of Validation Engineer jobs are:
What states have the most Contract Validation Engineer jobs? States with the most job openings for Contract Validation Engineer jobs include:
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Contract Validation Engineer jobs near you
Infographic showing various Contract Validation Engineer job openings in the United States as of June 2026, with employment types broken down into 45% Full Time, and 55% Contract. Highlights an 100% In-person job distribution, with an average salary of $108,152 per year, or $52 per hour.
MES Validation Engineer

MES Validation Engineer

Dawar Consulting, Inc.

Hillsboro, OR • Remote

$75 - $84/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 21 days ago

Job description

This is a remote position.

Our client, a world leader in the life sciences and diagnostics industry, is looking for a “MES Validation Engineer” in
Hillsboro, OR

Job Duration: Long Term Contract (Possibility Of Extension)
Pay Rate: $75/hr - $84/hr on W2 DOE
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

We are seeking an experienced MES Validation Engineer to support the deployment and validation of Manufacturing Execution Systems (MES) within a GMP-regulated biotechnology manufacturing environment. The successful candidate will be responsible for developing and executing validation strategies, protocols, and test scripts for computerized systems while ensuring compliance with FDA, EMA, GxP, and industry standards.

Key Responsibilities
  • Develop, author, review, and execute validation protocols, test scripts, and validation reports for MES and computerized systems.
  • Support implementation and validation of Rockwell FactoryTalk PharmaSuite and related manufacturing systems.
  • Collaborate with IT/OT, Quality Assurance, Manufacturing, System Owners, and Business Process Owners to ensure validation activities align with GMP requirements.
  • Develop validation strategies, risk assessments, traceability matrices, and testing plans.
  • Execute Computer System Validation (CSV) activities including IQ, OQ, PQ, UAT, and system qualification.
  • Ensure compliance with FDA, EMA, 21 CFR Part 11, GAMP 5, and Data Integrity requirements.
  • Support change controls, deviations, CAPA investigations, and audit readiness activities.
  • Manage testing execution, defect tracking, and validation deliverables throughout the project lifecycle.
  • Work with regulated systems such as MES, LIMS, SCADA, ERP, and electronic records systems.
  • Provide technical guidance on validation best practices and system compliance.
Required Qualifications
  • Bachelor's degree in Biomedical Engineering, Computer Science, Biology, Biochemistry, Chemistry, Biotechnology, Regulatory Affairs, Information Technology, or related Life Sciences field.
  • Minimum 5 years of experience in Computer System Validation (CSV) or Validation Engineering within a GMP-regulated environment.
  • Experience with Rockwell FactoryTalk PharmaSuite.
  • Strong knowledge of FDA, EMA, GxP, GAMP 5, and 21 CFR Part 11 requirements.
  • Experience authoring and executing validation protocols and test scripts.
  • Experience with risk assessments, change control, deviations, and CAPA processes.
  • Strong verbal and written communication skills.
  • Ability to work effectively in cross-functional teams.
Preferred Qualifications
  • Experience with ValGenesis, LIMS, SCADA, ERP systems, DeltaV, or other regulated manufacturing platforms.
  • Professional certifications such as CQE, CSQE, or CSVS.
  • Experience supporting MES implementation projects.
  • Knowledge of pharmaceutical, biotech, cell therapy, gene therapy, or biologics manufacturing operations.
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

If interested, please send your updated resume to hr@dawarconsulting.com/kavitha@dawarconsulting.com