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Final Quality Control Inspector Jobs in Raleigh, NC

This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross ...

This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross ...

Quality Control Technician

Oxford, NC · On-site

$45K - $55K/yr

Sample, inspect and disposition components and finished goods in accordance with department ... Enters final disposition in SAP. * Notifies appropriate personnel (supervisors, mechanics, and ...

Demonstrated expertise in Quality Control Inspection principles and regulatory administration with previous proven experience in a similar role: * Electronic/Electrical Inspection Methods and ...

Quality Inspector

Creedmoor, NC · On-site

$26 - $33/hr

Demonstrated expertise in Quality Control Inspection principles and regulatory administration with previous proven experience in a similar role: * Electronic/Electrical Inspection Methods and ...

Demonstrated expertise in Quality Control Inspection principles and regulatory administration with previous proven experience in a similar role: * Electronic/Electrical Inspection Methods and ...

Demonstrated expertise in Quality Control Inspection principles and regulatory administration with previous proven experience in a similar role: * Electronic/Electrical Inspection Methods and ...

Manage inspector resources including third party and direct-hire quality inspectors. * Provide overall project-wide oversight on quality and requirements compliance matters on QA/QC functions.

Manage inspector resources including third party and direct-hire quality inspectors. * Provide overall project-wide oversight on quality and requirements compliance matters on QA/QC functions.

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Final Quality Control Inspector information

See Raleigh, NC salary details

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$32

How much do final quality control inspector jobs pay per hour?

As of May 29, 2026, the average hourly pay for final quality control inspector in Raleigh, NC is $20.88, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $23.37 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Final Quality Control Inspector, and why are they important?

To thrive as a Final Quality Control Inspector, you need a keen eye for detail, strong understanding of quality assurance standards, and typically a high school diploma or technical certification. Familiarity with inspection tools (like calipers, micrometers), quality management systems (such as ISO 9001), and reporting software is commonly required. Excellent communication, critical thinking, and problem-solving skills help inspectors document findings and collaborate effectively with production teams. These skills are crucial to ensure products meet required specifications and maintain customer satisfaction and regulatory compliance.

What are some common challenges faced by Final Quality Control Inspectors, and how are they addressed on the job?

Final Quality Control Inspectors often face challenges such as identifying subtle defects in products under tight deadlines and maintaining consistency across large production batches. To address these, inspectors use standardized checklists, precision measuring tools, and collaborate closely with production teams to ensure clear communication about quality standards. Continuous training and adherence to quality protocols also help inspectors stay updated on best practices and improve their accuracy, making it easier to uphold rigorous quality requirements.

What does a Final Quality Control Inspector do?

A Final Quality Control Inspector is responsible for examining finished products to ensure they meet specified quality standards before they are shipped to customers. They inspect items for defects, verify compliance with safety and quality guidelines, and document any issues found during the inspection process. Their work helps ensure that only products meeting the company’s quality requirements reach the market, reducing returns and enhancing customer satisfaction. Final Quality Control Inspectors may also recommend improvements to production processes to prevent future defects.

What is the difference between Final Quality Control Inspector vs Quality Assurance Inspector?

AspectFinal Quality Control InspectorQuality Assurance Inspector
CertificationsOften requires quality control certifications (e.g., CQI, ASQ)May also hold similar certifications, with additional focus on QA processes
Work EnvironmentWorks at the end of production lines, inspecting finished productsInvolved throughout the production process, ensuring quality standards are met
Industry UsageCommon in manufacturing, aerospace, automotive sectorsUsed across manufacturing, pharmaceuticals, and food industries
Primary FocusDetects defects in finished products before shipmentDevelops and implements quality systems to prevent defects

While both roles focus on quality, the Final Quality Control Inspector primarily inspects finished products for defects, whereas the Quality Assurance Inspector works proactively to develop processes that prevent defects throughout production.

What are popular job titles related to Final Quality Control Inspector jobs in Raleigh, NC? For Final Quality Control Inspector jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Final Quality Control Inspector jobs in Raleigh, NC look for? The top searched job categories for Final Quality Control Inspector jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Final Quality Control Inspector jobs? Cities near Raleigh, NC with the most Final Quality Control Inspector job openings:

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Posted 23 days ago


Job description

Job Description
POSITION SUMMARY
The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site. This role is accountable for ensuing the generation of accurate, reliable, and compliant analytical data to support product release, stability, and lifecycle management in accordance with global GMP requirements.
The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.
POSITION RESPONSIBILITIES
  • Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.
  • Partner with AS&T to ensure the robustness and lifecycle management of the analytical control strategy including method qualification, validation, transfer, and performance monitoring.
  • Oversee analytical, microbiological, and environmental monitoring programs, ensuring compliance with GMP requirements and site contamination control strategy
  • Ensure data integrity, accuracy, and reliability of all QC data in accordance with regulatory expectations.
  • Establish and maintain inspection readiness, including hosting regulatory inspections and responding to health authority inquiries.
  • Drive timely and thorough investigations of OOS, OOT, and atypical results, ensuring appropriate root cause identification and effective CAPA implementation.
  • Ensure appropriate specifications, test methods, and acceptance criteria are established and maintained throughout the product lifecycle.
  • Oversee QC laboratory operations including resource planning, capacity management, and organizational capability development
  • Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support batch release, process improvements, and regulatory submissions.
  • Lead continuous improvement initiatives to enhance laboratory efficiency, compliance, and right-first-time performance.
  • Develop and monitor QC performance metrics, identifying trends and driving actions to improve performance and compliance.
  • Build and develop a high performing QC organization, fostering a strong quality culture and technical excellence.
  • Participates in business sub-teams as a Subject Matter Expert (SME) to provide input on timeliness and to address analytical/microbiological related issues
  • Other responsibilities and duties as the company may from time-to-time assign

EDUCATION AND EXPERIENCE
  • Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred.
  • Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles.
  • Strong leadership skills with experience building and leading high-performing technical teams.
  • Experience managing environmental monitoring and contamination control strategies in GMP manufacturing environments.
  • Experience supporting DS & DP manufacturing in GMP environments.
  • Proven track record of regulatory inspection success and audit management.
  • Proven experience with laboratory method lifecycle management.
  • Experience implementing or optimizing laboratory systems and processes preferred.

TECHNICAL SKILLS / CORE COMPETENCIES
  • Deep expertise in GMP regulations applicable to QC laboratories supporting ATMPs.
  • Strong knowledge of analytical techniques (e.g. q/rt/ddPCR, flow cytometry, ELISA, cell-based assays, microbiological methods) and their application tin DS/DP testing.
  • Strong understanding of data integrity principles and regulatory expectations (ALCOA+).
  • Ability to operate effectively in a matrixed, cross-functional environment.
  • Strong problem-solving skills with a risk-based and science-driven approach.
  • Excellent communication skills with the ability to influence at site and executive levels.
  • Strong project management skills.