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Qa Validation Jobs in Raleigh, NC (NOW HIRING)

QA Systems Specialist Location: Raleigh NC, fully onsite Monday-Friday 8am-5pm Salary Range: $76 ... Experience supporting validation, capital projects, equipment qualification, or process ...

Director of Quality Assurance Summary: Forge Battery is a rapidly growing company that is building ... robust quality validation and control plans. * Operate effectively in non-steady-state ...

Documenting validations of new test and measurement services. * Developing and monitoring QA performance indicators, reporting findings to management, and identifying areas for improvement.

New

Short Description: Sr. Software Tester; Sr. Quality Control Analyst; Sr. Quality Assurance Engineer ... for verifying and validating whether products or services meet specified requirements. The ...

Director of Quality Assurance Summary: Forge Battery is a rapidly growing company that is building ... robust quality validation and control plans. * Operate effectively in non-steady-state ...

Director of Quality Assurance Full‑time, Raleigh, NC Summary Forge Battery is a rapidly growing ... validation and control plans. * Operate effectively in non‑steady‑state manufacturing ...

Quality Assurance Engineer

Oxford, NC · On-site

$70K - $95K/yr

Quality * Assesses the impact of deviations, CAPAs, and associated change request on the validation status of equipment and/or systems. * Assist in defining, testing, and implementing comprehensive ...

Showing results 21-40

Qa Validation information

See Raleigh, NC salary details

$10

$54

$95

How much do qa validation jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for qa validation in Raleigh, NC is $54.74, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $68.46 per hour, depending on experience, location, and employer.

What are some common challenges faced by QA Validation professionals in regulated industries?

QA Validation professionals in regulated industries often face the challenge of staying current with evolving compliance standards while ensuring that all processes and documentation meet strict regulatory requirements. They must balance thorough validation activities with tight project timelines, often collaborating closely with cross-functional teams such as manufacturing, engineering, and regulatory affairs. Attention to detail and strong organizational skills are essential, as even small errors can lead to costly delays or regulatory findings. Effective communication with team members and stakeholders is also critical to ensure successful audits and product launches.

What is a QA Validation professional?

QA Validation professionals are specialists responsible for ensuring that products, processes, or systems meet defined quality standards and regulatory requirements. They design and execute tests, document results, and analyze data to confirm that all specifications are met before a product is released or a process goes live. Their work is crucial in industries such as pharmaceuticals, manufacturing, and software, where compliance and consistent quality are essential. QA Validation experts help prevent defects, ensure safety, and maintain customer trust.

What is the difference between Qa Validation vs Qa Analyst?

AspectQa ValidationQa Analyst
CertificationsGMP, GxP, Validation certificationsGMP, GxP, Quality assurance certifications
Work EnvironmentRegulated industries like pharma, biotechPharmaceutical, biotech, manufacturing
Primary FocusValidating processes, systems, equipmentAnalyzing quality data, audits, process improvements
Employer UsageQuality validation teams in regulated industriesQuality assurance departments across industries

Qa Validation specialists focus on validating systems and processes to ensure compliance with industry standards, often working on equipment and software validation. Qa Analysts primarily analyze quality data, perform audits, and support process improvements. While both roles ensure product quality, Qa Validation emphasizes validation activities, whereas Qa Analysts focus on ongoing quality analysis and reporting.

What are the key skills and qualifications needed to thrive as a QA Validation professional?

To thrive as a QA Validation professional, you need a solid understanding of quality assurance processes, regulatory standards (such as FDA or ISO), and a relevant science or engineering degree. Familiarity with validation protocols, documentation systems, and tools like LIMS or TrackWise is typically required, along with certifications such as ASQ CQV or similar. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring compliance and facilitating teamwork. These competencies are critical for guaranteeing product quality, regulatory compliance, and the smooth operation of validation activities in highly regulated industries.
Infographic showing various Qa Validation job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 8% Part Time, 1% Temporary, and 7% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $113,853 per year, or $54.7 per hour.

QA Systems Specialist

Kelly Services

Raleigh, NC

$76K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago


Job description

QA Systems SpecialistLocation: Raleigh NC, fully onsite
Monday-Friday 8am-5pm
Salary Range: $76,000-$110,000/year
Position Summary

The QA Systems Specialist is responsible for supporting Quality Assurance systems to ensure compliance with cGMP, FDA, and other applicable regulatory requirements. This role helps maintain inspection readiness by supporting quality systems, change control, audits, quality metrics, and continuous improvement initiatives. Working cross-functionally with Manufacturing, Quality Control, Engineering, Supply Chain, and Regulatory Affairs, the QA Systems Specialist promotes a culture of quality and operational excellence while ensuring products and processes meet established quality standards.

Key Responsibilities
  • Support and promote a culture of quality and regulatory compliance across the site.
  • Ensure compliance with cGMP, FDA, and applicable regulatory requirements.
  • Review quality documentation, including change controls, deviations, investigations, risk assessments, and related quality records.
  • Support the administration of the Change Control system, including reviews, approvals, KPI tracking, and documentation.
  • Collect, analyze, and report Quality Systems metrics for Management Review meetings and Annual Product Reviews (APRs).
  • Provide Quality Assurance oversight and guidance for quality systems activities and change control processes.
  • Identify and communicate quality risks, compliance concerns, and regulatory issues to management.
  • Support customer audits, regulatory inspections, and inspection readiness activities.
  • Participate in internal audits, document findings, and assist with corrective action follow-up.
  • Support employee training related to quality systems, cGMP requirements, and data integrity.
  • Maintain accurate quality records in accordance with company procedures and data integrity requirements.
  • Contribute to continuous improvement initiatives that strengthen quality systems and operational performance.
  • Perform additional duties as assigned.
QualificationsRequired
  • Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Engineering, or a related scientific discipline.
  • Minimum of five (5) years of experience in the pharmaceutical, biotechnology, or other cGMP-regulated industry.
  • Experience supporting Quality Systems, Quality Assurance, Manufacturing Quality, Validation, or related quality functions.
  • Experience participating in regulatory inspections, customer audits, and internal audits.
  • Experience with Change Control processes.
  • Strong understanding of Quality Systems, Quality Assurance principles, and regulatory compliance.
  • Excellent written, verbal, analytical, organizational, and interpersonal communication skills.
  • Proficiency with Microsoft Office applications (Word, Excel, Outlook, and PowerPoint).
Preferred
  • Working knowledge of cGMP, FDA, and international regulatory requirements.
  • Experience with electronic Quality Management Systems (eQMS), including Change Control, Deviations, CAPA, Document Control, and Training.
  • Experience supporting validation, capital projects, equipment qualification, or process implementation.
  • Knowledge of quality risk management and continuous improvement methodologies.
  • Familiarity with data integrity principles and 21 CFR Part 11.
  • Experience supporting Annual Product Reviews (APRs), Management Reviews, and quality metrics.
  • ASQ, RAPS, or other quality certifications are a plus.
Work Environment
  • Position is fully onsite within a pharmaceutical manufacturing environment.
  • Work includes office, laboratory, warehouse, and manufacturing areas.
  • Must be able to wear required PPE and comply with gowning requirements in controlled manufacturing environments.
  • Occasional overtime or schedule flexibility may be required to support audits, inspections, investigations, or business needs.
  • Regular collaboration with cross-functional teams is required to support quality and compliance objectives.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
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