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Contract Validation Engineer Jobs (NOW HIRING)

NKW NantKwest Inc

Validation Engineer III

Dunkirk, NY · On-site

... contracts, cost tracking and project cost projections. * Partner with engineering studies and investigation studies as applicable * Lead audits and regulatory agency inspections for Validation,

ImmunityBio

Validation Engineer III

Dunkirk, NY · On-site

... contracts, cost tracking and project cost projections. * Partner with engineering studies and investigation studies as applicable * Lead audits and regulatory agency inspections for Validation,

ImmunityBio, Inc.

Validation Engineer III

Dunkirk, NY · On-site

... contracts, cost tracking and project cost projections. * Partner with engineering studies and investigation studies as applicable * Lead audits and regulatory agency inspections for Validation,

Net Orbit

Customer Validation Engineer

Longmont, CO · On-site

Longmont, CO Role Type: long term contract/FTE • Perform product testing and failure analysis to support new product development • Experience of 2-4 yrs using SATA, SSD, NVMe. • System level ...

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How much do contract validation engineer jobs pay per hour?

As of Aug 10, 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?

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.

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Contract Validation Engineer jobs near you
Infographic showing various Contract Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 74% In-person, 13% Hybrid, and 13% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Equipment Validation Engineer

Automated Systems, Inc.

Tampa, FL • On-site

$45 - $65/hr

Contractor

Medical, Dental, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Equipment Validation Engineer

Location: Greater Tampa Bay Area, FL - onsite  

Contract: 6+ months duration with potential for extensions

Automated Systems Inc. is seeking an Equipment Validation Engineer to support one of our client’s pharmaceutical manufacturing operations in the Greater Tampa Bay Area, Florida. The Equipment Validation Engineer Contractor will develop, execute, and evaluate qualification and validation activities demonstrating that facilities, manufacturing equipment, packaging equipment, and associated processes operate consistently and in compliance with cGMP requirements. The role includes authoring and executing IQ/OQ/PQ protocols and summary reports, supporting validation project planning, and coordinating with Engineering, Manufacturing, Quality, Maintenance, and external vendors to integrate validation activities into project and production schedules.

Job Responsibilities

· Develop, execute, and analyze equipment and process validation projects supporting cGMP compliance.

· Author and execute IQ, OQ, and PQ protocols and associated summary reports for manufacturing and packaging equipment.

· Author or support change controls, SOPs, work instructions, and validation lifecycle documentation.

· Provide technical support for deviations, CAPAs, investigations, and equipment or process changes.

· Design and execute process and cleaning validation studies in accordance with site procedures and industry standards.

· Support equipment startup, product changeovers, troubleshooting, and continuous improvement initiatives.

· Coordinate with internal and external technical personnel to establish priorities, schedules, responsibilities, and practical validation approaches.

Relevant Equipment Experience

Experience with oral solid dose process and packaging equipment is desirable, including:

· Analytical equipment (HPLCs, Dissolution, etc.)

· Fluid bed dryers

· Granulators, including high-shear granulation equipment

· Pharmaceutical mills, including cone and hammer mills

· Bottle fillers

· Blister fillers

· Cappers

· Labelers and barcode systems

· Cartoners



Education and Skill Qualifications:


· Bachelor's degree in Engineering, Pharmacy, Science, or a related technical discipline.

· Two or more years of experience in life sciences engineering, manufacturing, or validation.

· At least one year of direct equipment qualification or validation experience.

· Experience working in an FDA-regulated, cGMP-compliant manufacturing environment.

· Experience with oral solid dose manufacturing or packaging equipment is strongly preferred.

· Strong technical writing, collaboration, communication, and organizational skills.

· Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.

Company Description

We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.