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Qa Validation Jobs in Raleigh, NC (NOW HIRING)

Fujifilm

QA Specialist, Validation

Holly Springs, NC · On-site

Position Overview The QA Specialist, Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance ...

New

Fujifilm

QA Specialist, Validation

Holly Springs, NC · On-site

The QA Specialist, Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance oversight, review ...

New

Fujifilm

QA Specialist, Validation

Holly Springs, NC

Position Overview The QA Specialist, Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance ...

Data Bridge Consultants

Senior QA Engineer

Cary, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Audits QA validation and verification procedures as directed * Makes recommendations to QA Engineers on validation and verification issues uncovered * Ensure application meets documented requirements ...

Data Bridge Consultants

Senior QA Engineer

Cary, NC

$40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Audits QA validation and verification procedures as directed * Makes recommendations to QA Engineers on validation and verification issues uncovered * Ensure application meets documented requirements ...

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 ... Experience in analytical method validation and QC testing, especially in the fields of mammalian ...

HirexHire

QA Engineer

Raleigh, NC · On-site

They are seeking a Quality Assurance Engineer to ensure the reliability and quality of a SaaS ... validate functionality, identify edge cases, and evaluate the overall user experience. • Build ...

HirexHire

QA Engineer

Raleigh, NC · Remote

Perform manual testing to validate functionality, identify edge cases, and evaluate the overall ... WHAT YOU WILL NEED * 3+ years of experience in Quality Assurance, Software Testing, or a similar ...

HirexHire

QA Engineer

Raleigh, NC · On-site

Perform manual testing to validate functionality, identify edge cases, and evaluate the overall ... WHAT YOU WILL NEED * 3+ years of experience in Quality Assurance, Software Testing, or a similar ...

HirexHire

QA Engineer

Raleigh, NC · Remote

Perform manual testing to validate functionality, identify edge cases, and evaluate the overall ... WHAT YOU WILL NEED * 3+ years of experience in Quality Assurance, Software Testing, or a similar ...

HirexHire

QA Engineer

Raleigh, NC · Remote

Perform manual testing to validate functionality, identify edge cases, and evaluate the overall ... WHAT YOU WILL NEED * 3+ years of experience in Quality Assurance, Software Testing, or a similar ...

Kryosphere

Be Seen First

Quality Assurance Specialist I

Cary, NC · On-site

$20 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... validation documentation and other facility forms * QA review clinical kits components/labeling, labeled components, and shipment of kits * Participate in internal audits * Client reports * Special ...

Posted today

Kryosphere

Be Seen First

Quality Assurance Specialist I

Cary, NC · On-site

$20 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... validation documentation and other facility forms * QA review clinical kits components/labeling, labeled components, and shipment of kits * Participate in internal audits * Client reports * Special ...

Posted today

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All JobsQa Validation JobsQa Validation Jobs in Raleigh, NC

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.

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

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

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

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

Qa Validation jobs near you
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 Specialist, Validation

Fujifilm

Holly Springs, NC • On-site

Other

Posted 3 days ago

New

Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

50th of 539 rated manufacturers

Job description

Position Overview
The QA Specialist, Validation is responsible for helping to drive the Quality oversight for commissioning and qualification processes. This role is responsible for quality assurance oversight, review, and approval of validation activities and documents associated with new systems, changes to existing systems, maintaining the validated state of equipment/processes/systems, and decommissioning.
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description
What You'll Do
  • Performs a role within the QA team for the development of documents, processes, and procedures for the Validation program.
  • 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 a validated state.
  • Provides oversight and approval of system and process lifecycle documentation, including risk and impact assessments, user requirements, product, process and equipment specifications, functional specifications, traceability matrices, qualification protocols, validation plans, and validation summary reports.
  • Generates, reviews, and approves QA procedures for the validation approach and lifecycle documents for facilities, utilities and equipment.
  • Generates, reviews, and approves QA documentation, procedures, and processes for QA support of manufacturing operations in cGMP regulated facility.
  • Ensures project and operational quality objectives are met within desired timelines.
  • Manufacturing (Clean Room) shop floor support for issue resolution, as needed.
  • Participates in optimization or improvement initiatives and supports regulatory agency and third-party inspections.
  • Must be flexible to support 24/7 manufacturing facility.
  • Performs other duties, as assigned.

Knowledge, Skills, and Abilities
  • Strong verbal and written communication skills to partner with different teams and stakeholders.
  • Excellent oral and written communications skills and fluency in English.
  • Strong time management, ability to meet tight deadlines to ensure effective prioritization of tasks.
  • Ability to think critically and have superior problem-solving skills.
  • Collaborative attitude with the willingness to work with global peers and cross-functional teams toward company and department goals.
  • Basic knowledge and application of cGMP compliance and other related regulations.
  • Fully embraces a Genki culture, able to bring positive energy to a dynamic work environment.
  • Occasional opportunity for International and/or Domestic travel may be available.

Minimum Qualifications
  • Bachelor's degree in Life Sciences or Engineering with 2 years of applicable industry experience; OR,
  • Master's degree in Life Sciences or Engineering with no previous experience.
  • 1-3 years of experience working in a GMP regulated environment.
  • Experience in Validation and/or Quality oversight, in an FDA regulated facility.

Preferred Qualifications
  • Working knowledge and experience with ASTM E2500, Smartsheets, Trackwise, Veeva, and Kneat validation software.
  • Familiarity/understanding of validation of production equipment, hygienic utilities, quality systems, automation, manufacturing & IT Systems, and methodologies.
  • Understanding of GAMP5, Data Integrity, and application of 21 CFR Part 820 and Part 11.
  • Understanding of Drug Substance, Drug Product and/or Finished Goods manufacturing processes.
  • Experience with startup projects or initiatives.
  • Training and/or familiarity with Quality Risk Management principles.

Physical Requirements:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is required on a regular basis to:
  • Ability to discern audible cues.
  • Ability to stand for prolonged periods of time for up to 120 minutes.
  • Ability to sit for prolonged periods of time for up to 120 minutes.
  • Ability to conduct activities using repetitive motions that include wrists, hands, and/or fingers.
  • Ability to conduct work that includes moving objects up to 10 pounds.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.
*LI-Onsite
EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

Social media

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