ZipRecruiter

Log In

2

Contract Validation Engineer Full Time Jobs in Raleigh, NC

TrueField Systems LLC

Chief Engineer

Raleigh, NC

TRUEFIELD SYSTEMS LLC Chief Engineer Full-Time • Early-Stage Startup • Field & Lab Environment ... Field Testing & Validation Plan and execute seasonal field test programs across the full target ...

TrueField Systems LLC

Chief Engineer

Raleigh, NC · On-site

TRUEFIELD SYSTEMS LLC Chief Engineer Full-Time • Early-Stage Startup • Field & Lab Environment ... Field Testing & Validation Plan and execute seasonal field test programs across the full target ...

Microsoft

Contract Administrator

Durham, NC · On-site

Within CO&I, the Engineering Procurement & Construction (EPC) organization is responsible for ... Support invoice validation and payment administration processes. * Track contract values, approved ...

Hitachi

Contract Management Professional

Raleigh, NC · On-site +1

$86K - $115K/yr

Legal, Compliance & Audit Job Schedule: Full time Remote: No The Opportunity At Hitachi Energy, we ... Strong knowledge of engineering, procurement, and service agreements. * Proven ability to manage ...

Hitachi, Ltd.

Contract Management Professional

Raleigh, NC · On-site

$86K - $115K/yr

Legal, Compliance & Audit Job Schedule: Full time Remote: No The Opportunity At Hitachi Energy, we ... Strong knowledge of engineering, procurement, and service agreements. * Proven ability to manage ...

Millennium Print Group

Industrial Systems Engineer

Raleigh, NC · On-site

$68K - $91K/yr

Research Triangle Park, NC Schedule: Full-time, Onsite Pay & Benefits: Competitive salary + bonus ... Analyze manufacturing scenarios to identify process improvements, validate engineering assumptions ...

Millennium Print Group

Industrial Systems Engineer

Raleigh, NC · On-site

$68K - $91K/yr

Research Triangle Park, NC Schedule: Full-time, Onsite Pay & Benefits: Competitive salary + bonus ... Analyze manufacturing scenarios to identify process improvements, validate engineering assumptions ...

Visium Resources, Inc.

Electrical Engineer

Raleigh, NC · On-site

Provide technical guidance into the design, project management, commissioning and validation, and ... Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe ...

City of Durham, NC

Senior Engineer

Durham, NC · On-site +1

$79K - $122K/yr

... Full time with benefits Remote Employment: Flexible/Hybrid Job Number: 26-05954 Department ... Valid North Carolina Class C Driver's License with a satisfactory driving record acquired within a ...

City of Durham, NC

Senior Engineer

Durham, NC · On-site +1

$79K - $122K/yr

... Full time with benefits Remote Employment: Flexible/Hybrid Job Number: 26-05953 Department ... Valid North Carolina Class C Driver's License with a satisfactory driving record acquired within a ...

Hitachi

Senior Contract Manager

Raleigh, NC · Hybrid

Legal, Compliance & Audit Job Schedule: Full time Remote: Yes Senior Contract Manager (m/f/d) To ... engineering projects * Knowledge of utility-scale EPC agreement (onshore and offshore) * Excellent ...

previous pagenext page

Showing results 21-40

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

Contract Validation Engineer Full Time information

See Raleigh, NC salary details

$21

$50

$75

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

As of Sep 6, 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

Project Manager - Senior CQV Pharmaceutical

Visium Resources, Inc.

Raleigh, NC • On-site

Full-time

Re-posted 20 days ago

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for a full time position as a Senior CQV Project Manager located in Raleigh, NC. We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This individual will oversee cross-functional CQV execution for GMP-regulated facilities, utilities, equipment, automation systems, and manufacturing processes while ensuring compliance with FDA, cGMP, and global regulatory standards.


The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison between engineering, quality, validation, manufacturing, and external vendors. This role requires the ability to manage project schedules, budgets, risks, resources, and validation deliverables in support of facility expansions, new product introductions, and operational readiness initiatives.


Key Success Criteria
  • Experience leading major expansion C&Q projects start to finish (brownfield or greenfield). From strategy / planning through to full doc prep & execution
  • Writes CQV Strategies & Plans.
  • CQV Schedule
  • Should have experience with C&Q of process equipment.
  • Has experienced with integrated CQV (ASTM E2500 and ISPE C&Q baseline guide)
  • Has experience with digital validation (i.e. Kneat or other software) is a major asset but not required.
  • Capital Improvements experience is a major asset but not required.

Key Responsibilities
  • Lead all CQV project activities for pharmaceutical and biotech manufacturing projects. 
  • Develop and manage CQV strategies, project plans, schedules, budgets, and resource allocation. 
  • Coordinate commissioning and qualification activities for: 
    • Process equipment 
    • Clean utilities 
    • HVAC systems 
    • Automation and control systems 
    • Manufacturing and packaging lines 
  • Ensure compliance with FDA, cGMP, ISPE, GAMP, and corporate quality standards. 
  • Oversee execution of: 
    • FAT/SAT protocols 
    • IQ/OQ/PQ protocols 
    • Validation documentation 
    • Deviations and CAPAs 
    • Change controls 
  • Collaborate with Quality Assurance, Engineering, Manufacturing, Automation, and Regulatory teams to support project milestones and inspection readiness. 
  • Manage third-party CQV consultants, contractors, and vendors. 
  • Provide risk assessments and mitigation strategies to maintain project timelines and compliance objectives. 
  • Support startup, operational readiness, and technology transfer activities. 
  • Present project status updates and KPI reporting to senior leadership and stakeholders.

Qualified candidates would have the following:

  • Minimum 8-12 years of experience in pharmaceutical, biotech, or life sciences industries. 
  • Minimum 5 years of direct CQV project management experience within GMP-regulated manufacturing environments. 
  • Proven experience managing large-scale capital projects, facility expansions, or greenfield startup projects. 
  • Strong experience with commissioning and qualification of: 
    • Cleanrooms 
    • Process equipment 
    • Utilities 
    • Automation systems 
    • Manufacturing processes 
  • Experience authoring and reviewing validation lifecycle documentation. 
  • Demonstrated success leading cross-functional teams and managing multiple project workstreams simultaneously. 
  • Experience supporting FDA audits and regulatory inspections. 
  • Background in biologics, sterile fill-finish, vaccine, API, or aseptic manufacturing environments strongly preferred. 

Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related technical discipline. 
  • Strong understanding of: 
    • cGMP regulations 
    • FDA validation requirements 
    • ISPE Baseline Guides (inc. C&Q) and ASTM E2500 GUIDE
    • GAMP 5 principles 
  • Proficiency with project management methodologies, scheduling tools, and reporting systems. 
  • Excellent communication, leadership, and stakeholder management skills. 
  • Ability to work effectively in fast-paced, highly regulated project environments. 

Preferred Qualifications
  • Digital Validation software experience (i.e. Kneat or equivalent)
  • PMP certification preferred. 
  • Experience with DeltaV, MES, SCADA, or other pharmaceutical automation platforms. 
  • Familiarity with Kneat, TrackWise, Veeva, or electronic validation systems. 
  • Previous consulting or EPCM experience is a plus. 
  • Lean Six Sigma certification preferred.

________________________________________________________________________________________________


Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company's success is based on your success. When you work with us, you are never 'just a number'. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium.
Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.