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Validation Jobs in Raleigh, NC (NOW HIRING)

Valspec

Process Validation Engineer

Raleigh, NC · On-site

$70 - $80/hr

Valspec--a global provider of system validation and lifecycle services--provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999 ...

Eupry

Validation Team Manager (Raleigh, NC)

Raleigh, NC · On-site

Validation Team Manager (Raleigh, NC) Are you an inspiring leader with a passion for quality and compliance? Eupry is on the hunt for a Validation Team Manager to lead our dynamic validation team in ...

CAI

Senior Validation Engineer

Raleigh, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

CAI

Senior Validation Engineer

Raleigh, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines. This ...

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How much do validation jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for validation in Raleigh, NC is $46.48, according to ZipRecruiter salary data. Most workers in this role earn between $35.24 and $56.49 per hour, depending on experience, location, and employer.

What is a validation job?

A validation job involves verifying that systems, processes, or products meet specified standards and requirements. It often includes tasks such as testing, documentation, and compliance checks, especially in industries like pharmaceuticals, manufacturing, and software development.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What engineers make $500,000?

Senior engineers in specialized fields such as software, petroleum, or aerospace engineering can earn $500,000 or more annually, often with extensive experience, advanced skills, and sometimes stock options or bonuses. High-level roles typically require advanced degrees, certifications, and leadership responsibilities within their organizations.

How to become a validation specialist?

To become a validation specialist, typically one needs a background in science, engineering, or a related field, along with experience in quality assurance or manufacturing processes. Certifications such as GxP validation or Six Sigma can enhance prospects, and familiarity with regulatory standards like FDA or ISO is often required. Strong attention to detail and knowledge of validation tools and documentation are essential for success in this role.

Do validation engineers make good money?

Validation engineers typically earn competitive salaries that vary based on experience, industry, and location. They often require knowledge of quality assurance, testing procedures, and tools like GxP or validation software, which can influence compensation levels.

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 or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What are validation jobs?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Raleigh, NC? The most popular types of Validation jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Validation jobs? Cities near Raleigh, NC with the most Validation job openings:
Validation jobs near you
Infographic showing various Validation job openings in Raleigh, NC as of July 2026, with employment types broken down into 55% Full Time, 17% Part Time, and 28% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $96,672 per year, or $46.5 per hour.

Advanced Quality / Validation Engineer

NNE AS

Clayton, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

Job description

As an Advanced CQV Consultant you are responsible for the planning, execution, and delivery of commissioning, qualification, and validation (CQV) activities within pharmaceutical, biotechnology, and life science projects. This role independently executes complex CQV deliverables while serving as the Project Quality Manager (PQM) on assigned projects, ensuring quality, compliance, and validation strategies are aligned with customer requirements, industry standards, and regulatory expectations. The consultant works as part of multidisciplinary project teams and serves as a subject matter expert in CQV, quality risk management, GMP compliance, and validation lifecycle activities from project initiation through handover.
Primary Duties and Responsibilities:
About the job: The Advanced CQV Consultant is a senior-level validation and quality professional responsible for leading commissioning, qualification, and validation (CQV) activities across pharmaceutical and life sciences projects. This role combines hands-on technical expertise with Project Quality Management responsibilities, ensuring facilities, equipment, systems, and processes meet GMP, regulatory, and client requirements. Working closely with multidisciplinary teams and customer stakeholders, the consultant serves as a trusted advisor on validation strategy, compliance, risk management, and quality execution. The ideal candidate brings deep CQV experience, strong leadership skills, and a passion for delivering high-quality, compliant project outcomes.
Key Responsibilities
CQV Execution
  • Lead commissioning, qualification, and validation (CQV) activities for facilities, utilities, equipment, and computerized systems.
  • Develop and review CQV lifecycle documentation, including validation plans, risk assessments, IQ/OQ/PQ/PfV protocols, traceability matrices, and summary reports.
  • Execute qualification activities, troubleshoot technical and compliance challenges, and ensure compliance with GMP regulations, industry standards, and company procedures.
  • Collaborate with engineering, automation, quality, and manufacturing teams while supporting FAT, SAT, startup, and commissioning activities.
  • Identify and escalate project risks, scope changes, and compliance concerns.

Project Quality Management
  • Serve as Project Quality Manager (PQM) on small to mid-sized projects, defining and managing validation and quality deliverables.
  • Align project quality strategies with client expectations and regulatory requirements, while monitoring budgets, resources, risks, and quality outcomes.
  • Support Quality Assurance Plans (QAPs), facilitate GMP, GEP, ASTM E2500, and design reviews, and provide quality oversight across project disciplines.
  • Act as a trusted advisor to both project teams and clients on quality and compliance matters.

Client, Leadership & Business Support
  • Build strong client relationships and provide technical guidance on CQV and validation strategies.
  • Support proposals, project planning, cost estimates, and business development activities.
  • Present project progress, risks, and mitigation plans to stakeholders and leadership.
  • Mentor junior consultants, promote validation and quality best practices, and contribute to knowledge-sharing and continuous improvement initiatives.

Required Qualifications:
EducationBachelor's or Master's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field.
Experience & Knowledge
  • 8+ years of CQV, Quality, Validation, or GMP consulting experience within the pharmaceutical, biotechnology, or life sciences industry.
  • Experience leading qualification and validation programs for GMP-regulated facilities.
  • Experience as a Quality Lead, Validation Lead, or Project Quality Manager on complex projects.
  • Strong knowledge of GMP regulations (FDA, EMA, ICH), GAMP 5, ASTM E2500, ISPE Baseline Guides, Quality Risk Management, Data Integrity, and Validation Lifecycle Management.

Preferred Qualifications
  • Experience supporting large capital projects, clean utilities, process equipment, facilities, and automation systems.
  • PMP, ASQ, ISPE, or similar professional certification.
  • Client-facing consulting experience.

What we offer you
  • Competitive salary with annual adjustment increases
  • 160 hours of PTO (prorated from hire date) + 14 paid holidays
  • Health, dental, and vision insurance from day one
  • 8% guaranteed 401(k) company contribution
  • 14 weeks paid parental leave
  • Company-paid life and disability insurance
  • Employee referral bonuses

Please submit your application online. Please note that we only accept applications submitted via our online system.
Deadline of application is 7/31/2026
Wewill invite to interviews on a running basis.

Apply