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Quality Control Manager Jobs in Raleigh, NC (NOW HIRING)

Actalent

Senior QC Sample Management Lead

Raleigh, NC · On-site

$40 - $60/hr

The ideal candidate brings a combination of hands-on QC sample management experience and process/system development expertise, with the ability to drive cross-functional alignment and scalable ...

GlaxoSmithKline

QC Group Leader

Zebulon, NC

Ensure that the QC testing and method validation of all products/value streams is performed to GMP ... Adopt participative management style that empowers the team by involving them in setting objectives ...

JT International S.A.

Quality Control Operator

Chapel Hill, NC · On-site

$15.50 - $19/hr

Manage various tasks and projects as they arise and upon manager's request Requirements: * An Associate's degree or a relevant experience in quality control, manufacturing, or a similar industry may ...

Intellectt INC

Quality Control Inspector

Durham, NC · On-site

Quality Control Inspector Location: 1106 Roche Drive, Durham, NC 27703 Duration: 3 months Work days/hours: M - F 7:30am - 4:30pm Onsite daily Description * Responsible for the efficient and effective ...

Actalent

QC Sample Coordinator

Raleigh, NC

$19.25 - $26.50/hr

Job Title: QC Sample Coordinator The QC Sample Coordinator supports Quality Control Chemistry and Microbiology testing by managing end-to-end sample logistics and documentation in a GMP environment.

Actalent

QC Sample Coordinator

Raleigh, NC · On-site

$19.25 - $26.50/hr

Job Title: QC Sample Coordinator The QC Sample Coordinator supports Quality Control Chemistry and Microbiology testing by managing end-to-end sample logistics and documentation in a GMP environment.

IntelliPro Group Inc.

QC Analyst I

Durham, NC · On-site

$30.48/hr

Durham, NC, 27709 Pay rate: $30.48/hr. on W2 Position Summary The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on ...

IntelliPro Group Inc.

QC Analyst I

Durham, NC · On-site

Durham, NC, 27709 Pay rate: $30.48/hr. on W2 Position Summary The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on ...

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Quality Control Manager information

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$29.6K

$79K

$125.9K

How much do quality control manager jobs pay per year?

As of May 30, 2026, the average yearly pay for quality control manager in Raleigh, NC is $79,049.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,800.00 and $97,200.00 per year, depending on experience, location, and employer.

What Does a Quality Control Manager Do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.

What are the biggest challenges a Quality Control Manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

More about Quality Control Manager jobs
What are the most commonly searched types of Quality Control jobs in Raleigh, NC? The most popular types of Quality Control jobs in Raleigh, NC are:
What are popular job titles related to Quality Control Manager jobs in Raleigh, NC? For Quality Control Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Quality Control Manager jobs in Raleigh, NC look for? The top searched job categories for Quality Control Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Quality Control Manager jobs? Cities near Raleigh, NC with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Raleigh, NC as of May 2026, with employment types broken down into 66% Full Time, 29% Part Time, and 5% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $79,049 per year, or $38 per hour.

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Posted 25 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.

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