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Director Quality Control Jobs (NOW HIRING)

haeco

Director, QC & Chief Inspector

Greensboro, NC

The Director of Quality Control/Chief Inspector is responsible for providing guidance with and in compliance with all FAA rules and regulations applicable to AAR granted under Title 14 of the Code of ...

HAECO

Director, QC & Chief Inspector

Greensboro, NC · On-site

The Director of Quality Control/Chief Inspector is responsible for providing guidance with and in compliance with all FAA rules and regulations applicable to AAR granted under Title 14 of the Code of ...

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Director Quality Control information

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$31K

$125.6K

$213.5K

How much do director quality control jobs pay per year?

As of Jul 23, 2026, the average yearly pay for director quality control in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

How much does a QA director make in the US?

A Quality Assurance (QA) Director in the US typically earns between $100,000 and $160,000 annually, depending on experience, industry, and location. Senior roles with extensive experience and certifications can earn higher salaries, often exceeding $180,000. Compensation may also include bonuses and benefits related to leadership and quality management skills.

Is QC a high paying job?

Quality Control (QC) roles, including positions like Director of Quality Control, tend to offer competitive salaries that increase with experience, industry, and location. Senior QC positions often have higher pay, especially when combined with certifications such as Six Sigma or ISO standards, and may include additional benefits depending on the company.

What does a director of quality control do?

A director of quality control oversees the quality assurance processes within an organization, ensuring products or services meet company standards and regulatory requirements. They develop quality policies, lead testing and inspection activities, analyze data to identify issues, and implement improvements, often managing teams and working with cross-functional departments.

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.

Which pays more, QA or QC?

For a Director of Quality Control, salaries are generally comparable to those of Quality Assurance directors, but QA roles often have higher pay due to broader responsibilities and strategic planning. Compensation depends on industry, experience, and location, with QA roles sometimes offering higher salaries for leadership positions. Both roles may require certifications like Six Sigma or ISO standards, which can influence pay scales.

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 cities are hiring for Director Quality Control jobs? Cities with the most Director Quality Control job openings:
What are the most commonly searched types of Quality Control jobs? The most popular types of Quality Control jobs are:
What states have the most Director Quality Control jobs? States with the most job openings for Director Quality Control jobs include:
Director Quality Control jobs near you
Infographic showing various Director Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.
Senior Director, Quality Control

Senior Director, Quality Control

ProKidney

Winston Salem, NC • On-site

Full-time

Posted 3 days ago

Job description

The Sr Director of Quality Control will be responsible for leadership of the various functional responsibilities of the Quality Control department, including QC - Operations, QC - Incoming Raw Materials, QC - Systems & Services, and QC - Microbiology Sterility Assurance. The role will lead continuous improvement activities of all quality control systems and drive a continued state of inspection readiness. The leader in this role must ensure that quality documentation and controls are effectively in place for phase III investigational new drugs (investigational medicinal products) to meet all quality requirements and regulatory standards and meet continuous clinical supply and delivery expectations leading to commercialization.
Essential Duties & Responsibilities:
  • Directs the development, validation, planning, implementation, and maintenance of QC product tests and analytical methods, processes, and operations.
  • Supports the design and execution of the environmental monitoring and sterility assurance programs for GMP manufacturing operations.
  • Supports development of QC tests and analytical methods that support production, including design support
  • Validates analytical test methods for raw materials and finished goods
  • Oversees raw material, in-process and final product release testing.
  • Responsible for ensuring the appropriate stability programs are initiated and completed to support product development and customer requirements.
  • Ensures quality control systems and equipment are compliant with standards and applicable regulatory guidelines
  • Responsible for ensuring that project objectives are met & continuous improvement of the Analytical Laboratories.
  • Strong scientific background and experience with cellular therapies across a broad range of cell types and disease treatments (adult-derived cells, stem cells, immune cells. allogeneic, autologous, etc.)
  • Familiarity with applicable regulatory requirements and compendia concerning cGMP manufacturing and testing of human cells (21CFR210, 211, 820 and 1271; Eudralex, USP, EP and ICH).
  • Understanding of analytical method qualification and validation per USP, EP and ICH guidelines.
  • Responsible for developing and delivering training materials to ensure that all QC employees' operational, scientific, and analytical training is conducted as needed to ensure that the group is entirely and accurately trained on time for all QC activities.
  • Responsible for liaison with the Manufacturing, Quality Assurance, Supply Chain, Project Management, Facilities, and other GMP Quality Control units.
  • Provide support in resolving issues to meet project goals and deliverables.
  • Serves as primary QC contact for regulatory inspections.
  • Leads and participates in projects within the organization's objectives and project timelines and participates in cross-functional projects as the quality control subject matter expert.
  • Hires, manages, and trains staff. Plans and assigns duties to meet departmental and organizational objectives. Provides guidance and direction to staff, including appropriate training, mentoring, and development of staff.
  • Mentor's direct reports and guide them to the next level in their careers
  • Is the primary point of contact and SME for analytical testing and provides guidance aligned with regulatory standards and good laboratory practices.

Qualifications:
  • Education/Training: Bachelor's degree in biology, biochemistry, immunology, molecular and cellular biology, or a related scientific discipline required. Advanced degree or Ph.D. in a scientific or technical discipline preferred.
  • Experience: 10+ years of experience in a GMP-regulated biopharmaceutical environment, including 10+ years in a management or leadership role. Experience in biologics or cell therapy preferred.
  • Knowledge: Strong knowledge of cGMP manufacturing and testing requirements for human cells, including 21 CFR 210, 211, 820, and 1271; EudraLex; USP; EP; and ICH guidelines. Understanding of analytical method qualification and validation per USP, EP, and ICH guidelines.
  • Skills: Advanced root cause investigation, troubleshooting, laboratory data evaluation, risk management, project leadership, communication, relationship-building, and team leadership skills. Proficiency with Microsoft Word, PowerPoint, and Excel required.
  • Certifications/Licenses: N/A

ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.
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About ProKidney

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

Winston-Salem, NC, US

Year founded

2019

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