ZipRecruiter

Log In

1

Verification And Validation Engineer Jobs in Raleigh, NC

Analog Devices

Verification SW Engineer

Durham, NC · On-site

$131K/yr

Verification SW Engineer INTRODUCTION The System Validation Group ( SVG ) at Analog Devices is looking for a Software Engineer to develop test suites to validate a growing family of very ...

CRB

CQV Engineer III

Raleigh, NC · On-site

... validation activities * Witness and verify FAT/SAT, test protocols, and qualification execution ... Mentor and train junior engineers and project team members on CQV best practices * Track, report ...

CRB

CQV Engineer III

Raleigh, NC

... validation activities * Witness and verify FAT/SAT, test protocols, and qualification execution ... Mentor and train junior engineers and project team members on CQV best practices * Track, report ...

CRB

CQV Engineer III

Raleigh, NC · On-site

... validation activities * Witness and verify FAT/SAT, test protocols, and qualification execution ... Mentor and train junior engineers and project team members on CQV best practices * Track, report ...

Analog Devices

Verification SW Engineer

Durham, NC · On-site

They are seeking a Verification SW Engineer to develop test suites for validating sophisticated Wireless Battery Management System products and networking products within the Automotive ...

next page

Showing results 1-20

All JobsVerification And Validation Engineer JobsVerification And Validation Engineer Jobs in Raleigh, NC

Verification And Validation Engineer information

See Raleigh, NC salary details

$21

$50

$75

How much do verification and validation engineer jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for verification and 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.

What are the key skills and qualifications needed to thrive as a Verification and Validation Engineer, and why are they important?

To thrive as a Verification and Validation Engineer, you need a solid background in engineering principles, software or hardware testing methodologies, and a relevant degree such as in electrical, computer, or systems engineering. Familiarity with test automation tools (e.g., Selenium, Jenkins), scripting languages, and standards like ISO or IEEE V&V processes is commonly required, along with certifications such as ISTQB. Attention to detail, analytical thinking, and strong communication skills set top performers apart by enabling thorough test coverage and clear reporting. These skills are essential to ensure products meet quality standards, regulatory requirements, and customer expectations before release.

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

AspectVerification And Validation EngineerQuality Assurance Engineer
CredentialsTypically requires engineering degrees, certifications like ISTQB or ASQ CQEOften holds degrees in engineering, quality management, or related fields; certifications like Six Sigma or ISTQB
Work EnvironmentWorks in product development, testing labs, and manufacturing settingsWorks across development, production, and process improvement environments
Industry UsageCommon in electronics, aerospace, automotive, and medical device industriesWidely used in manufacturing, software, and service industries
FocusEnsures products meet specifications through testing and validationEnsures quality processes are followed to prevent defects

While both roles aim to ensure product quality, Verification And Validation Engineers focus on testing and confirming that products meet specifications, whereas Quality Assurance Engineers develop and maintain quality systems and processes to prevent defects. Both roles often collaborate but serve different stages of the product lifecycle.

How does a Verification and Validation Engineer typically interact with development and QA teams during a project?

A Verification and Validation Engineer works closely with both development and QA teams to ensure that products meet specified requirements and function as intended. They often review design documents, develop test plans, and execute test cases in collaboration with developers, providing feedback on potential issues early in the process. Regular communication and coordination with QA are essential to ensure comprehensive test coverage and resolve defects efficiently. This collaborative approach helps maintain product quality and supports a smooth development lifecycle.

What are Verification and Validation Engineers?

Verification and Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified requirements and function as intended. They design and execute tests, review documentation, and analyze results to confirm that deliverables are both built correctly (verification) and serve their intended purpose (validation). Their work is crucial in highly regulated industries like aerospace, automotive, and healthcare, where safety and compliance are critical. These engineers collaborate with development teams to identify defects early and help ensure that projects meet quality standards before release.
What are popular job titles related to Verification And Validation Engineer jobs in Raleigh, NC? For Verification And Validation Engineer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Verification And Validation Engineer jobs in Raleigh, NC look for? The top searched job categories for Verification And Validation Engineer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Verification And Validation Engineer jobs? Cities near Raleigh, NC with the most Verification And Validation Engineer job openings:
Verification And Validation Engineer jobs near you
6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer

6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer

Verista, Inc.

Apex, NC • On-site

$107K - $168K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

Job description

Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

We are seeking aClean-in-Place (CIP) CQV Engineer with hands-on experience overseeing the commissioning and qualification of Clean-In-Place (CIP) systems. This role ensures that all systems are designed, tested, and documented in alignment with project requirements and safety standards.
Clean-in-Place (CIP) CQV Engineer Responsibilities:
CIP System Leadership
  • Serve as the commissioning and qualification (C&Q) lead for CIP systems (responsibilities described below).
  • Develop and optimize CIP cleaning cycles to meet operational and quality standards.
  • Supervise the safe introduction and handling of caustic solutions during cleaning cycle development.
C&Q Lead Responsibilities
Commissioning and Qualification Documentation
  • Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications.
  • Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
  • Engage with design engineers and SMEs to clarify system intent and operational requirements.
  • Ensure alignment with quality, automation, and engineering teams on critical parameters and documentation.
  • Create Commissioning Test Plans that translate design intent into testable steps.
  • Coordinate with the Automation Team to incorporate all automation functional testing.
  • Collaborate with SMEs to ensure system requirements are accurately reflected in test plans.
  • Develop Installation, Operational, and Qualification (IOQ) protocols.
  • Prepare and submit summary reports documenting commissioning and qualification activities.
System Ownership and Execution
  • Take custody of the system post-construction and maintain ownership through C&Q completion.
  • Perform Lockout/Tagout (LOTO) for system safety.
  • Conduct pre-startup safety checks and risk assessments.
  • Prepare daily pre-task plans and verify team readiness for safe execution.
  • Attend daily commissioning meetings to coordinate activities.
  • Execute commissioning and IOQ protocols.
  • Resolve issues arising during execution.
  • Participate in Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) as required.
Requirements:
  • Bachelor's degree in Engineering, Biotechnology, Life Sciences, or a related technical discipline
  • 10+ years of role-specific experience
  • Experience supporting CQV activities within GMP-regulated pharmaceutical or biotechnology environments
  • Hands-on experience with CIP systems and automated cleaning processes
  • Strong understanding of CQV lifecycle documentation (IQ/OQ/PQ protocols and reports)
  • Ability to work independently while coordinating with cross-functional project teams
  • Strong technical documentation and communication skills
  • Experience using digital validation platforms such as Kneat
  • Experience supporting FAT/SAT, commissioning, and equipment startup
  • Familiarity with automated process systems and PLC-based equipment
  • Experience in biologics or large-scale biopharmaceutical manufacturing environments
  • Onsite job requirement in Apex, NC

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range
$107,800-$168,011 USD
Benefits
Why Choose Verista?
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com

Apply