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Contract Validation Engineer Full Time Jobs in Raleigh, NC

Pinnaql

Validation Engineer

Holly Springs, NC · On-site

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

Valspec

Process Validation Engineer

Raleigh, NC

Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking an experienced Process Engineer to support process validation and Process Performance ...

Valspec

Process Validation Engineer

Durham, NC

Contract | Full-Time (40 Hours/Week) Duration: Approximately 9 Months Position Summary Our client is seeking an experienced Process Engineer to support process validation and Process Performance ...

New

Valspec

Process Validation Engineer

Raleigh, NC

$70 - $80/hr

Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... Contract / consulting -- initial term approximately 12 months, with a possibility of extension ...

Visium Resources, Inc.

Be Seen First

Pharmaceutical Senior CQV Engineer

Raleigh, NC · On-site

$125K - $150K/yr

Validation test scripts * Traceability matrices * Summary reports * Support startup and ... Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe ...

New

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All JobsContract Validation Engineer JobsContract Validation Engineer Full Time JobsContract Validation Engineer Full Time Jobs in Raleigh, NC

Contract Validation Engineer Full Time information

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

As of Aug 13, 2026, the average hourly pay for contract validation engineer full time 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 the difference between Contract Validation Engineer Full Time vs Contract Quality Assurance Engineer?

AspectContract Validation Engineer Full TimeContract Quality Assurance Engineer
CredentialsEngineering degree, certifications in validation or testingEngineering or related degree, QA certifications often preferred
Work EnvironmentManufacturing, medical devices, or software industriesManufacturing, software, or healthcare sectors
Employer UsageUsed by companies needing validation of products/processesUsed by organizations ensuring product quality and compliance

Contract Validation Engineers Full Time focus on verifying that products meet specifications through validation processes, often in regulated industries. Contract Quality Assurance Engineers also ensure product quality but emphasize testing, inspections, and compliance. While both roles require similar credentials and work environments, their core responsibilities differ slightly, with validation engineers concentrating on validation protocols and QA engineers on quality assurance processes.

What are popular job titles related to Contract Validation Engineer Full Time jobs in Raleigh, NC?

For Contract Validation Engineer Full Time jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Contract Validation Engineer Full Time jobs in Raleigh, NC look for?

The top searched job categories for Contract Validation Engineer Full Time jobs in Raleigh, NC are:

Contract Validation Engineer Full Time jobs near you

Validation Engineer

Validation & Engineering Group, Inc

Holly Springs, NC

Full-time

Re-posted 15 hours ago

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.