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Validation Engineer Jobs in Raleigh, NC (NOW HIRING)

CAI

Validation Engineer

Raleigh, NC

$72K - $80K/yr

... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus ...

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

PSC Biotech

Senior Validation Engineer

Durham, NC

$120K - $140K/yr

Your Role We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical ...

PSC Biotech

Senior Validation Engineer

Durham, NC · On-site

Your Role We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical ...

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

Oxford Biomedica

Validation Engineer III

Durham, NC · On-site

We are currently recruiting for a Validation Engineer III to join our Engineering Team. In this role, you will support Engineering, Manufacturing, Quality Control, and Facilities teams by executing ...

Valspec

Process Validation Engineer

Raleigh, NC · On-site

$70 - $80/hr

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement:

CAI

Senior Validation Engineer

Raleigh, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Raleigh, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

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How much do validation engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for validation engineer in Raleigh, NC is $50.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.32 and $61.44 per hour, depending on experience, location, and employer.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often working in industries like pharmaceuticals, biotech, or manufacturing. The role typically requires knowledge of regulatory requirements, validation protocols, and tools like GxP or SOPs, and can offer stable employment with opportunities for advancement. Job satisfaction depends on individual interests in quality assurance, technical skills, and industry stability.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of regulatory standards and experience with validation tools are also important.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

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

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

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

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.
More about Validation Engineer jobs
What are the most commonly searched types of Validation Engineer jobs in Raleigh, NC? The most popular types of Validation Engineer jobs in Raleigh, NC are:
What are popular job titles related to Validation Engineer jobs in Raleigh, NC? For Validation Engineer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Validation Engineer jobs in Raleigh, NC look for? The top searched job categories for Validation Engineer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Validation Engineer jobs? Cities near Raleigh, NC with the most Validation Engineer job openings:
Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Raleigh, NC as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $105,127 per year, or $50.5 per hour.

Equipment Validation Engineer

Alliance Biotech Solutions LLC

Raleigh, NC • On-site

Full-time

Dental, Vision, Retirement, PTO

Re-posted 8 days ago

Job 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.

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