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Validation Jobs in Raleigh, NC (NOW HIRING)

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

Validation Engineer (CQV)

Holly Springs, NC

Validation Engineer (CQV) Location: Raleigh-Durham area, NC Position Overview We are seeking an experienced Validation Engineer (CQV) to support commissioning, qualification, and startup activities ...

Valspec

Validation Engineer (CQV)

Raleigh, NC

Validation Engineer (CQV) Location: Raleigh-Durham area, NC Position Overview We are seeking an experienced Validation Engineer (CQV) to support commissioning, qualification, and startup activities ...

VDart, Inc.

Silicon Validation Engineer

Raleigh, NC · On-site

Silicon Validation Engineer Location: Raleigh, North Carolina (Onsite) Type: Full Time * Manage lab servers, test benches, and associated hardware infrastructure * Perform system provisioning ...

CAI

Validation Engineer

Raleigh, NC

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

Aston Carter

Data Validation Specialist

Raleigh, NC · On-site

$22.50/hr

Data Validation Specialist Engage in customer and account data entry for both new and existing accounts. Validate data by identifying inconsistencies, errors, duplicates, and missing information. Use ...

CAI

Validation Engineer

Raleigh, NC

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

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How much do validation jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for validation 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.

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 $105,133 per year, or $50.5 per hour.

Validation Engineer III

Oxford Biomedica

Durham, NC • On-site

Full-time

Posted 5 days ago

Job description

Join Us in Changing Lives
Full time, On-site
At OXB, our people are at the heart of everything we do. We're on a mission to enable life-changing therapies to reach patients around the world-and we're looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us.
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 initial validation and qualification of equipment, utilities, facilities, and systems, as well as implementing the requalification and periodic review program. You will play a key role in advancing our mission and making a meaningful difference.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.
Your responsibilities in this role would be:
  • Write, execute, summarize and lead validation activities for: Analytical instruments, Computer Systems (as applicable to complex instruments and manufacturing equipment),Equipment, Utilities, and Facilities.
  • Development of Validation Plans and Validation Plan Summary Reports.
  • Develop, review, and provide guidance on internal validation documents.
  • Develop, support, and assess CAPAs, Change Controls, Deviations, Investigations and Risk Management as they pertain to validation.
  • Provide technical input to strategy/philosophy for validation activities.
  • Represent validation during tech transfer activities.
  • Front facing during agency inspections client audits representing the validation function.
  • Lead and manage complex validation and technical projects.
  • Provide technical support for troubleshooting, improving, or optimizing ongoing manufacturing operations, including being on-call for after-hours remote support.

We are Looking For:
  • Minimum of bachelor's degree in science, engineering or related discipline.
  • 5+ years of experience in the execution of validation studies in a regulated manufacturing environment.
  • Thorough knowledge and understanding of FDA and international health authority expectations.
  • Experience in authoring and review/approval of CQV documentation including validation plans, protocols, reports, trace matrices and SOPs

About Us:
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.
OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us?
  • Competitive total reward packages
  • Wellbeing programs that support your mental and physical health
  • Career development opportunities to help you grow and thrive
  • Supportive, inclusive, and collaborative culture
  • State-of-the-art labs and manufacturing facilities
  • A company that lives its values: Responsible, Responsive, Resilient, Respect

We want you to feel inspired every day. At OXB, we're future-focused and growing fast. We succeed together-through passion, commitment, and teamwork.
Ready to Make a Difference?

Apply