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Full Time Validation Engineer Jobs (NOW HIRING)

LG Electronics

Validation Engineer II

Aliso Viejo, CA · On-site

$70K - $94K/yr

Validation Engineer II * Perform validation for infotainment/telematic products by utilizing test ... Recruiting Range $70,725-$94,300 USD Benefits Offered Full-Time Employees: * No-cost employee ...

Agilent

Process Validation Engineer

Frederick, CO

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Agilent

Process Validation Engineer

Frederick, CO · On-site

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Agilent

Process Validation Engineer

Boulder, CO

$105K - $164K/yr

As a Process Validation Engineer within the Process Validation team of Agilent's Advanced ... The full-time equivalent pay range for this position is $105,280.00 - $164,500.00/yr plus ...

Hitachi, Ltd.

FDA Validation Engineer

Nashville, TN · On-site

Engineering & Science Job Schedule: Full time Remote: No JR Automation, a Hitachi Group Company ... Join us as an FDA Validation Engineer. Location type: This is an onsite position based in Nashville ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... for full-time employees including: * Health, dental and vision insurance * Life, AD&D and ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... for full-time employees including: * Health, dental and vision insurance * Life, AD&D and ...

LG Electronics

Sr. Validation Engineer

Aliso Viejo, CA · On-site

$87K - $116K/yr

Lead and guide validation engineers from a project execution perspective * Serves as the primary ... Recruiting Range $87,112-$116,150 USD Benefits Offered Full-Time Employees: * No-cost employee ...

Hitachi

FDA Validation Engineer

Nashville, TN

Engineering & Science Job Schedule: Full time Remote: No JR Automation, a Hitachi Group Company ... Join us as an FDA Validation Engineer. Location type: This is an onsite position based in Nashville ...

Oxford Biomedica

Validation Engineer III

Durham, NC · On-site

Join Us in Changing Lives Full time, On-site At OXB , our people are at the heart of everything we ... We are currently recruiting for a Validation Engineer III to join our Engineering Team. In this ...

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Full Time Validation Engineer information

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How much do full time validation engineer jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for full time 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 key skills and qualifications needed to thrive as a Full Time Validation Engineer, and why are they important?

To thrive as a Full Time Validation Engineer, you need a solid background in engineering principles, quality assurance, and validation processes, typically supported by a degree in engineering or a related field. Familiarity with industry standards (such as GMP or FDA regulations), data analysis tools, and validation software like ValGenesis or TrackWise is commonly required. Strong attention to detail, analytical thinking, and effective communication skills set top performers apart in this role. These capabilities ensure that products and processes consistently meet regulatory standards and quality expectations, which is critical for compliance and operational success.

What are some common challenges faced by Full Time Validation Engineers, and how can they be addressed?

Full Time Validation Engineers often encounter challenges such as tight project deadlines, evolving regulatory requirements, and the need to coordinate with cross-functional teams. Managing documentation and ensuring thorough testing while maintaining compliance can also be demanding. To address these challenges, it's important to stay organized, communicate proactively with colleagues in quality assurance, manufacturing, and R&D, and keep up-to-date with industry standards and regulations. Leveraging project management tools and regular team meetings can help streamline validation activities and minimize potential bottlenecks.

What is the difference between Full Time Validation Engineer vs Validation Technician?

AspectFull Time Validation EngineerValidation Technician
CredentialsBachelor's in Engineering or related field, certifications like GxP or IQ/OQ/PQAssociate's or Bachelor's, often with on-the-job training
Work EnvironmentDesigning validation protocols, analyzing data, overseeing validation processesExecuting validation tests, collecting data, supporting validation activities
Industry UsagePharmaceutical, biotech, medical device manufacturingSimilar industries, often as support staff
Search & ComparisonOften compared for roles involving validation planning and oversightCompared for hands-on testing and data collection roles

The Full Time Validation Engineer typically leads validation projects, requiring more technical expertise and planning skills, while the Validation Technician focuses on executing validation tests and supporting validation activities. Both roles are essential in regulated industries like pharmaceuticals and biotech, but they differ in responsibilities and required credentials.

What are Full Time Validation Engineers?

Full Time Validation Engineers are professionals who work to ensure that products, systems, or processes meet specified requirements and function as intended. They design and execute tests, analyze data, and document results to demonstrate compliance with regulatory standards and internal quality guidelines. Validation Engineers are commonly employed in industries such as pharmaceuticals, biotechnology, manufacturing, and electronics, where product safety and consistency are critical. Their role is crucial in preventing defects and ensuring that products are safe and effective for their intended use.
More about Full Time Validation Engineer jobs
What cities are hiring for Full Time Validation Engineer jobs? Cities with the most Full Time Validation Engineer job openings:
What are the most commonly searched types of Validation Engineer jobs? The most popular types of Validation Engineer jobs are:
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Full Time Validation Engineer jobs near you
Infographic showing various Full Time Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Equipment Validation Engineer

Alliance Biotech Solutions LLC

Raleigh, NC • On-site

Full-time

Dental, Vision, Retirement, PTO

Re-posted 18 days ago

Job description

Description:

Alliance Biotech Solutions has multiple openings for Validation Engineers to support the execution and coordination of commissioning, qualification, and validation (CQV) activities for new and existing equipment within a GMP-regulated CDMO environment. These roles will focus on the introduction of new process equipment and updates to existing systems, ensuring all validation activities are executed in compliance with FDA, GMP, and global regulatory standards.


This Validation Engineer will work cross-functionally with Manufacturing, Quality, Engineering, and Automation teams to support equipment qualification, system integration, and potential CSV activities. The role requires strong technical writing, analytical thinking, and hands-on execution to ensure compliant, efficient project delivery within aggressive timelines.

Requirements:

• Execute and support equipment qualification activities including IQ/OQ/PQ protocol development, execution, and report generation
• Support validation efforts for single-use systems including single-use mixers (SUMs), process pumps, and filtration systems (SUTFF)
• Participate in the qualification of lab instruments such as cell viability analyzers (e.g., Vi-Cell BLU) including potential CSV/data integrity support
• Perform on-the-floor validation execution including system walkdowns, functional testing, and coordination with operations
• Support system integration activities, ensuring equipment and instrumentation operate within defined parameters
• Assist with updates and modifications to existing systems, including parameter and instrumentation changes
• Investigate deviations, discrepancies, and non-conformances; perform root cause analysis and support corrective actions
• Ensure timely closure of validation deliverables and associated documentation
• Collaborate with cross-functional teams to align validation activities with project timelines and operational priorities
• Author and review validation protocols, reports, and technical documentation
• Support execution within electronic validation and quality systems (e.g., KNEAT, TrackWise, Veeva or similar)

Experience/Skills

• 2+ years (mid-level) or 5+ years (senior) of experience supporting CQV/validation activities in GMP-regulated environments
• Experience with equipment qualification (IQ/OQ/PQ) for manufacturing and/or lab systems
• Exposure to single-use technologies and/or biopharmaceutical manufacturing environments preferred
• Experience with CSV and data integrity concepts is a plus
• Strong understanding of GMP regulations and global compliance standards
• Ability to interpret technical documentation including P&IDs, URS, and process flow diagrams
• Strong technical writing and documentation skills
• Demonstrated analytical and problem-solving capabilities
• Ability to work independently and manage multiple priorities in a fast-paced project environment
• Strong communication skills with the ability to collaborate cross-functionally


Benefits & Compensation

• Competitive wage as a full-time employee

• Paid Time Off

• Dental and Vision Insurance with low employee cost

• paid long term and short-term disability

• 401K plan with employer contributions


About Alliance Biotech Solutions

Alliance Biotech Solutions (ABS) is a premier consulting firm specializing in biopharmaceutical engineering and validation services. As industry leaders in Commissioning, Qualification, and Validation (CQV), we provide crucial services to the biotech and pharmaceutical sectors while maintaining our philosophy that employees are our #1 priority. Our success is built on the foundation of empowering our team members' growth and development, recognizing that our employees are the cornerstone of our clients' success.