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

Cellectis

Director, Quality Control

Raleigh, NC · On-site

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 ...

Cellectis

Director, Quality Control

Raleigh, NC · On-site

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 ...

AskBio

Quality Control Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Quality Control Analyst I will be responsible for performing routine GMP testing on analytical ...

AskBio

Quality Control Analyst

Durham, NC

$23.25 - $31.25/hr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Quality Control Analyst I will be responsible for performing routine GMP testing on analytical ...

AskBio

Quality Control Analyst II

Durham, NC · On-site

$23.25 - $31.25/hr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Quality Control Analyst II will be responsible for performing routine testing on analytical ...

AskBio

Quality Control Analyst II

Durham, NC

$23.25 - $31.25/hr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Quality Control Analyst II will be responsible for performing routine testing on analytical ...

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All JobsDirector Quality Control JobsDirector Quality Control Jobs in Raleigh, NC

Director Quality Control information

See Raleigh, NC salary details

$30.1K

$122.1K

$207.5K

How much do director quality control jobs pay per year?

As of Jun 17, 2026, the average yearly pay for director quality control in Raleigh, NC is $122,094.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,500.00 and $146,800.00 per year, depending on experience, location, and employer.

What does a Director of Quality Control do?

A Director of Quality Control is responsible for overseeing the quality assurance and quality control processes within an organization. They develop and implement policies, procedures, and standards to ensure products or services meet regulatory and company requirements. This role involves managing teams, conducting audits, and working closely with other departments to resolve quality issues. The Director also analyzes data to identify trends and areas for improvement, ensuring continuous enhancement of quality systems.

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

To thrive as a Director of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and management, typically supported by a degree in science or engineering and substantial industry experience. Familiarity with quality management systems (QMS) like ISO 9001, Six Sigma certification, and proficiency in data analysis tools are often required. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional collaboration and continuous improvement. These competencies ensure product quality, regulatory adherence, and operational excellence in highly regulated industries.

What are some common challenges faced by a Director of Quality Control, and how can they be addressed?

Directors of Quality Control often encounter challenges such as maintaining compliance with evolving regulatory standards, managing cross-functional teams, and ensuring consistent product quality across multiple locations. To address these challenges, it's important to stay updated on industry regulations, foster open communication between departments, and implement robust training and quality management systems. Regular audits, data-driven decision making, and strong leadership are also key to overcoming obstacles and ensuring continuous improvement within quality control operations.
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 cities near Raleigh, NC are hiring for Director Quality Control jobs? Cities near Raleigh, NC with the most Director Quality Control job openings:
Director Quality Control jobs near you
Infographic showing various Director Quality Control job openings in Raleigh, NC as of June 2026, with employment types broken down into 75% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $122,094 per year, or $58.7 per hour.

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Posted 12 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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