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Equipment Validation Engineer Jobs (NOW HIRING)

Pinnaql

Validation Engineer - Upstream

Juana Diaz, PR · On-site

We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the ...

Actalent

Validation Engineer

Baltimore, MD

Validation Engineer The Validation Engineer manages and prioritizes all phases of assigned ... Lead and support equipment validation activities associated with manufacturing bulk drug substance ...

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How much do equipment validation engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for equipment validation engineer in the United States is $63.77, according to ZipRecruiter salary data. Most workers in this role earn between $52.64 and $69.71 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an equipment validation engineer, and why are they important?

To thrive as an Equipment Validation Engineer, you need a strong background in engineering principles, process validation, and regulatory standards such as GMP, typically supported by a degree in engineering or a related field. Familiarity with validation protocols (IQ/OQ/PQ), data analysis software, and documentation systems is essential, and certifications like Six Sigma or CQE can be advantageous. Attention to detail, strong problem-solving skills, and effective communication are critical soft skills for this role. These competencies ensure equipment operates reliably and compliantly, supporting product quality and regulatory approval in highly regulated industries.

What is the difference between Equipment Validation Engineer vs Quality Assurance Engineer?

AspectEquipment Validation EngineerQuality Assurance Engineer
CertificationsGMP, GxP, Validation certificationsISO, Six Sigma, QA certifications
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesManufacturing, software, service industries
Primary FocusValidating equipment and systems for complianceEnsuring product quality and process adherence

The Equipment Validation Engineer primarily focuses on validating equipment and systems to meet regulatory standards, ensuring operational compliance. In contrast, the Quality Assurance Engineer concentrates on maintaining overall product quality and process improvements. Both roles are essential in regulated industries but serve different aspects of quality management.

How does an equipment validation engineer typically collaborate with cross-functional teams during a validation project?

As an Equipment Validation Engineer, you will regularly work alongside quality assurance, manufacturing, engineering, and regulatory teams. Your role involves gathering input from these departments to develop comprehensive validation protocols and ensure equipment meets necessary standards. Effective communication and project management skills are essential, as you'll coordinate timelines, document results, and ensure that all stakeholders are aligned throughout the validation process. This collaborative environment offers valuable exposure to various functions within the organization and fosters both technical and interpersonal skill development.

What is an equipment validation engineer?

Equipment Validation Engineers are professionals responsible for ensuring that manufacturing equipment and systems operate according to required specifications and regulatory standards. They develop and execute validation protocols, conduct equipment testing, and document results to demonstrate compliance with industry guidelines, such as those set by the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and medical devices, where validated equipment is critical to product safety and quality.
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Equipment Validation Engineer jobs near you
Infographic showing various Equipment Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $132,650 per year, or $63.8 per hour.

Equipment Validation Engineer

ASI Systems Engineering

Tampa, FL • On-site

Full-time

Posted 19 days ago

Job description


Equipment Validation Engineer
Location: Tampa, FL - onsite
Contract: 6 months
Job Summary
ASI is seeking an Equipment Validation Engineer to support oral solid dose pharmaceutical manufacturing operations in Tampa, Florida. The engineer 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.
Relevant Equipment Experience
Experience with oral solid dose process and packaging equipment is desirable, including:
• 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
• Case packers
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.
Requirements
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.

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