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Validation Manager Jobs in Raleigh, NC (NOW HIRING)

Assesses the impact of system and process modifications and maintains oversight of change management processes to ensure facilities, utilities and equipment are first validated and then maintained in ...

Assesses the impact of system and process modifications and maintains oversight of change management processes to ensure facilities, utilities and equipment are first validated and then maintained in ...

Proficiency with quality management systems (QMS) and validation documentation practices. * Strong analytical, problem-solving, and organizational skills with high attention to detail. * Excellent ...

Assesses the impact of system and process modifications and maintains oversight of change management processes to ensure facilities, utilities and equipment are first validated and then maintained in ...

Senior Validation Engineer

Raleigh, NC · On-site

$87K - $120K/yr

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

... Management - Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities - Coordinate with project contractors and equipment vendors to execute required ...

Develop, execute, and manage validation plans for Microsoft D365 implementations and upgrades to ensure regulatory compliance, particularly in the cloud. * Compliance with Regulatory Standards:

Showing results 41-60

Validation Manager information

See Raleigh, NC salary details

$46.2K

$102.5K

$156K

How much do validation manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for validation manager in Raleigh, NC is $102,466.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $128,300.00 per year, depending on experience, location, and employer.

What is a validation manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a validation manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a validation manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

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 are popular job titles related to Validation Manager jobs in Raleigh, NC?

For Validation Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Validation Manager jobs in Raleigh, NC look for?

The top searched job categories for Validation Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Validation Manager jobs?

Cities near Raleigh, NC with the most Validation Manager job openings:

Infographic showing various Validation Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $102,466 per year, or $49.3 per hour.

Staff Compliance Validation Engineer

Cutera Inc.

Raleigh, NC • On-site

$130K - $150K/yr

Full-time

Posted 7 days ago


Job description

Position Summary:
We are seeking an experienced Compliance and Validation Engineer to lead validation strategy and execution across products, embedded software, hardware, and manufacturing processes. This role is critical to ensure that our technologies meet global regulatory requirements while maintaining the high standards of performance, scalability, and reliability.
As a key partner to R&D and Manufacturing, you will drive a proactive, engineering-focused approach to validation supporting new product introductions (NPI), design transfers, and sustaining operations. This role focuses on executing effective validation activities and supporting the development of efficient, scalable, and audit-ready processes.
Duties & Responsibilities:
  • Lead the development and execution of validation strategies, protocols, and reports for equipment, systems, software, and manufacturing processes.
  • Own and drive qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on production readiness.
  • Ensure compliance with applicable regulatory and quality standards (e.g., FDA, ISO 13485) through practical, engineering-driven validation approaches.
  • Partner cross-functionally with R&D and Manufacturing teams to support new product introduction (NPI), design verification/validation, and design transfer to production.
  • Support integration and validation of hardware/software systems, including test method development and execution.
  • Drive validation activities for manufacturing equipment, fixtures, and process development to ensure robust and repeatable production.
  • Author, review, and maintain validation documentation, ensuring accuracy, completeness, and audit readiness.
  • Support internal and external audits and regulatory inspections, serving as a subject matter expert for validation and compliance activities.
  • Develop and maintain SOPs and related documentation and deliver training to ensure consistent understanding and application of validation and compliance requirements.
  • Drive continuous improvement in validation and manufacturing processes, leveraging data-driven and engineering best practices.
  • Monitor evolving regulatory requirements and industry best practices, recommending and implementing improvements as needed.
  • Other duties as needed or required.

Minimum Requirements & Qualifications:
  • Bachelor's degree in Engineering, Quality, or a related field; advanced degree preferred
  • 8+ years of experience in validation engineering, quality, or compliance within a regulated industry (medical device, pharmaceutical, or biotechnology preferred).
  • Strong knowledge of validation principles, including IQ/OQ/PQ, with hands-on experience in software, hardware, and manufacturing environments.
  • Solid understanding of regulatory requirements and quality standards, including FDA regulations and ISO 13485.
  • Experience with embedded systems, hardware/software integration, and production test methodologies.
  • Familiarity with supporting NPI, design transfer, and manufacturing process validation.
  • Proficiency with quality management systems (QMS) and validation documentation practices.
  • Strong analytical, problem-solving, and organizational skills with high attention to detail.
  • Excellent communication and collaboration skills, with the ability to work effectively across engineering and manufacturing teams.

Preferred Qualifications:
  • Enterprise Architect
  • Markdown
  • Quarto
  • PowerShell, JavaScript, Typst (and other tools) for automating document generation.