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Director Quality Jobs in Raleigh, NC (NOW HIRING)

Cellectis

Director, Quality Control

Raleigh, NC

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 ...

Xylem

Sr. Director, Quality, MCS

Morrisville, NC · On-site

We are seeking a Senior Director of Quality to lead the MCS segment's quality strategy and ensure that our products, services, and operations meet or exceed industry standards, regulatory ...

Indivior

Director, Site Quality - Raleigh

Raleigh, NC · On-site

Director, Site Quality - Raleigh WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision ...

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Director Quality information

See Raleigh, NC salary details

$30.1K

$122.1K

$207.5K

How much do director quality jobs pay per year?

As of Jul 19, 2026, the average yearly pay for director quality 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 do?

A Director of Quality oversees the quality assurance and quality control processes within an organization to ensure that products or services meet established standards and regulatory requirements. They develop and implement quality management systems, lead teams responsible for inspections and audits, and work closely with other departments to promote continuous improvement. The Director of Quality also analyzes quality data, manages compliance with industry regulations, and often interacts with customers or external auditors to address quality concerns.

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

To succeed as a Director of Quality, you need extensive knowledge in quality management systems, regulatory compliance, and process improvement, often supported by a bachelor's or master's degree in a relevant field. Familiarity with tools such as Six Sigma, ISO standards, and quality auditing software, along with certifications like CQE or Six Sigma Black Belt, is typical. Exceptional leadership, analytical thinking, and effective communication are critical soft skills for driving quality initiatives and leading cross-functional teams. These competencies ensure organizational standards are upheld, continuous improvement is achieved, and regulatory risks are minimized.

What is the difference between Director Quality vs Quality Manager?

AspectDirector QualityQuality Manager
CredentialsBachelor's or Master’s in Quality Management, Engineering, or related field; certifications like ASQ CQE or CQABachelor's in Quality, Engineering, or related; certifications like ASQ CQE or CQA often preferred
Work EnvironmentStrategic leadership in quality initiatives, overseeing multiple departments or sitesOperational focus, managing daily quality processes and teams
Employer & Industry UsageUsed in manufacturing, healthcare, aerospace, and industries with complex quality systemsCommon in manufacturing, production, and service industries

The main difference between a Director Quality and a Quality Manager lies in their scope and strategic focus. The Director Quality typically oversees the entire quality program at a higher level, setting policies and long-term goals, while the Quality Manager handles daily operations and implements quality procedures. Both roles require similar credentials and certifications, but their responsibilities and strategic influence differ significantly.

How does a Director of Quality typically collaborate with cross-functional teams to drive continuous improvement initiatives?

A Director of Quality plays a key role in partnering with departments such as manufacturing, engineering, supply chain, and regulatory affairs to identify and resolve process inefficiencies and ensure compliance with quality standards. They often lead cross-functional meetings, facilitate root cause analyses, and champion a culture of continuous improvement by implementing best practices and quality tools like Six Sigma or Lean methodologies. Effective communication and the ability to influence stakeholders at all levels are essential, as the Director of Quality ensures that all departments are aligned with organizational quality goals and regulatory requirements.
What are the most commonly searched types of Quality jobs in Raleigh, NC? The most popular types of Quality jobs in Raleigh, NC are:
What are popular job titles related to Director Quality jobs in Raleigh, NC? For Director Quality jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Director Quality jobs in Raleigh, NC look for? The top searched job categories for Director Quality jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Director Quality jobs? Cities near Raleigh, NC with the most Director Quality job openings:
Director Quality jobs near you

Director, Quality Control

Cellectis

Raleigh, NC

Other

Re-posted 14 days ago

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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