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Qa Director Jobs in Raleigh, NC (NOW HIRING)

Cellectis

Director, Clinical Quality Assurance

Raleigh, NC · On-site

$190K - $2M/yr

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Director of Quality Assurance Summary: Forge Battery is a rapidly growing company that is building a multi-GWh battery plant in Morrisville, NC, and is seeking a highly skilled and experienced ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Director of Quality Assurance Summary: Forge Battery is a rapidly growing company that is building a multi-GWh battery plant in Morrisville, NC, and is seeking a highly skilled and experienced ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Director of Quality Assurance Summary: Forge Battery is a rapidly growing company that is building a multi-GWh battery plant in Morrisville, NC, and is seeking a highly skilled and experienced ...

Forge Nano Inc.

Director of Quality Assurance

Raleigh, NC · On-site

$120 - $160/hr

Director of Quality Assurance Full‑time, Raleigh, NC Summary Forge Battery is a rapidly growing company building a multi‑GWh battery plant in Morrisville, NC. The Director of Quality Assurance ...

NC SECU

VP QA Engineering

Raleigh, NC · On-site

Essential Responsibilities: * (30%) Direct and oversee QA teams and their adherence to all aspects of Software Testing Lifecycle driving an automation first quality mindset. Manage organizational ...

JobRx, Inc.

Senior Director of Quality

Morrisville, NC · On-site

$150 - $190/hr

The Senior Director of Quality Assurance is responsible for development and maintenance of quality business strategy and quality management system compliant with FDA drugs, biologics and combination ...

Aerogen Ltd

Senior Director of Quality

Morrisville, NC · On-site

The Senior Director of Quality Assurance is responsible for development and maintaining of quality business strategy and quality management system compliant with FDA drugs, biologics and combination ...

Allegiance Staffing

Quality Assurance

Cary, NC

$18.50/hr

Quality Assurance Employment Type: Full-Time Location: Cary, NC Pay: $18.50 per hour Schedule: Rotating Nights, 7:00 PM - 7:00 AM Job Summary: The Quality Assurance Technician is responsible for ...

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 ... Collaborate successfully with the other departments to ensure that direct and supportive tasks are ...

Adecco

Quality Assurance

Morrisville, NC

$18.50 - $18.88/hr

For Quality Assurance in Durham, Cary, and Morrisville - RTP. These opportunities come with competitive pay, weekly paychecks, benefits, and room for advancement. If you're looking for a stable job ...

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All JobsQa JobsQa Director JobsQa Director Jobs in Raleigh, NC

Qa Director information

See Raleigh, NC salary details

$54.9K

$136.2K

$221.1K

How much do qa director jobs pay per year?

As of Aug 13, 2026, the average yearly pay for qa director in Raleigh, NC is $136,172.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,100.00 and $164,300.00 per year, depending on experience, location, and employer.

What are some common challenges a QA director faces when building and leading a quality assurance team?

A QA Director often encounters challenges such as aligning quality goals with rapidly changing project requirements, balancing manual and automated testing strategies, and ensuring effective communication between QA teams and other departments like development and product management. Additionally, recruiting and retaining skilled QA professionals, fostering a culture of continuous improvement, and keeping up with evolving industry standards are frequent hurdles. Successful QA Directors address these challenges by promoting collaboration, investing in team training, and implementing scalable QA processes.

What are the key skills and qualifications needed to thrive as a QA director, and why are they important?

To thrive as a QA Director, you need deep expertise in quality assurance methodologies, leadership experience, and a background in computer science or a related field. Familiarity with test automation tools, QA management systems, and relevant certifications like ISTQB or Six Sigma are commonly expected. Strong strategic thinking, effective communication, and the ability to inspire and manage cross-functional teams are standout soft skills. These qualifications ensure the delivery of high-quality products, streamlined QA processes, and alignment between quality goals and overall business objectives.

What does a QA director do?

A QA Director, or Quality Assurance Director, is responsible for overseeing the entire quality assurance process within an organization. They develop and implement testing strategies, ensure products meet quality standards, and lead teams of QA professionals. The QA Director works closely with other departments to identify quality issues and drive continuous improvement. Their role is crucial in delivering reliable, high-quality products to customers.

What are the most commonly searched types of Qa jobs in Raleigh, NC?

The most popular types of Qa jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Qa Director jobs?

Cities near Raleigh, NC with the most Qa Director job openings:

Qa Director jobs near you
Infographic showing various Qa Director job openings in Raleigh, NC as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $136,172 per year, or $65.5 per hour.

Director, Clinical Quality Assurance

Cellectis

Raleigh, NC • On-site

$190K - $2M/yr

Full-time

Re-posted 6 days ago

Job description


The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable global and national regulatory requirements across Cellectis' clinical programs. This role provides strategic and operational quality leadership in alignment with other departments and company goals. They develop and implement a comprehensive Clinical Quality Assurance framework that safeguards patient safety, data integrity, and regulatory compliance throughout the clinical development lifecycle. The Director, Clinical Quality Assurance, will manage activities and projects based on short-term and long-term company goals. This position is also part of the Global Cellectis Quality Leadership team actively contributing to the overall global Quality strategy and initiatives.
Position Responsibilities
  • Defines and executes the Clinical QA strategy throughout the development trajectory including early-phase and late stage clinical development
  • Oversees GCP compliance for all clinical activities, including monitoring, data management, and pharmacovigilance
  • Develop and implement inspection readiness plans and procedures ensuring that clinical studies and related activities are ready for Health Authority inspections
  • Direct risk-based quality planning and continuous improvement initiatives across clinical programs
  • Manage vendor qualifications, audits, and corrective/preventive actions (CAPAs)
  • Collaborate cross-functionally to integrate quality principles into clinical development and regulatory deliverables
  • Provide training and guidance to cross-functional teams on GCP regulations, Quality Assurance procedures, and audit protocols
  • Develops quality strategies and priorities for short- and long-term objectives for the QA organization.
  • In collaboration with internal stakeholders, ensure risk-based quality management is applied as appropriate to specific studies
  • Facilitate review of potential Serious Breach and Urgent Safety Measure assessments arising from clinical program
  • Plan, coordinate, review, and approve clinical audits using risk-informed strategy to ensure compliance in clinical studies and pharmacovigilance operations
  • Implement and run internal GCP audit and training programs
  • Serve as a subject matter expert on GCP quality assurance matters
  • Develop KPIs to track and trend key Quality Indicators and ensures that any adverse trends or patterns are noted and are promptly addressed
  • Travel up to 10% of the time
  • Such other responsibilities and duties as the Company may from time-to-time assign

Education and Experience
  • Bachelor's or master's degree in science preferably in a Life Science, with at least twelve (12) years of relevant GCP, PV, and QA experience in a biopharmaceutical company. 8+ years of direct supervisory experience.
  • Extensive clinical trial experience in biological therapies and in oncology, ideally in CAR-T therapies and hemato-oncology.
  • Experience supporting IND, CTA, and BLA/MAA or other regulatory submissions.

Technical Skills / Core Competencies
  • Demonstrated ability to identify critical program risks and develop plans, strategic or tactical, to mitigate risks and costs. Knowledge and understanding of regulations regarding cell/gene therapies including but not limited to ICH guideline, GCP, and GMP as defined by the US Food and Drug Administration and European Medicines Agency.
  • Comprehensive knowledge of cell and gene therapy, GxPs, and the theories and general principles behind them.
  • Comprehensive knowledge of compliance with GCP worldwide regulations. Strong project management skills.
  • Demonstrated ability to lead, motivate, and influence a strategic direction. Ability to effectively leverage and develop diverse perspectives and ideas from matrix teams.
  • Ability to independently lead initiatives, assess complex challenges, and implement practical solutions.
  • Strong written and verbal communication skills. Bilingual in French and English preferred.
  • Ability to set and manage priorities and schedule activities accordingly. Strong analytical and problem-solving skills.
  • Demonstrated interpersonal skills to work effectively with subordinates, peers, managers, and cross-functional teams.
  • Excellent organizational skills with attention to detail and deadlines.
  • Strong team orientation including the ability to coach and mentor.

Anticipated Compensation Range: $190,000 - $234,0000

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