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

IQVIA

Associate Director, Medical Writing

Durham, NC · On-site

The Associate Director is a key leadership position responsible for determining and driving the ... Accountable for medical writing deliverable quality and ensures adherence to departmental ...

IQVIA

Associate Director, Medical Writing

Durham, NC · On-site

The Associate Director is a key leadership position responsible for determining and driving the ... Accountable for medical writing deliverable quality and ensures adherence to departmental ...

IQVIA

Associate Director, Medical Reviewer

Durham, NC · Remote

$115K - $322K/yr

Associate Director, Medical Review (MLR) Location : Home-based in USA Job Overview: IQVIA Pharma ... In this role and as part of the Medical Quality and Compliance team you will be working alongside ...

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Associate Director Quality information

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$10

$26

$49

How much do associate director quality jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for associate director quality in Raleigh, NC is $26.18, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $30.62 per hour, depending on experience, location, and employer.

What does an associate director quality do?

An Associate Director of Quality oversees quality assurance and quality control processes within an organization, ensuring that products or services meet established standards and regulatory requirements. They lead teams responsible for developing, implementing, and maintaining quality management systems, and often collaborate with other departments to drive continuous improvement. Additionally, they analyze quality data, handle audits, and provide training to staff on best practices. This role is critical for maintaining compliance, customer satisfaction, and the overall integrity of the company's offerings.

What are the key skills and qualifications needed to thrive as an associate director quality?

To thrive as an Associate Director of Quality, you need a thorough understanding of quality management systems, regulatory compliance, and relevant industry standards, usually supported by a bachelor's or master's degree in a scientific or engineering discipline. Familiarity with quality-related tools such as Six Sigma, ISO standards, and electronic quality management systems (eQMS) is typically required, along with certifications like ASQ or Lean Six Sigma. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills and qualities are vital to ensure product quality, regulatory adherence, and operational excellence within the organization.

What are some typical challenges faced by an associate director quality, and how can they be addressed?

As an Associate Director of Quality, one common challenge is balancing regulatory compliance with operational efficiency, especially when implementing new quality systems or updates. Navigating cross-functional communication and ensuring all departments adhere to quality standards can also be demanding, as it requires strong leadership and negotiation skills. Staying current with evolving industry regulations and effectively managing audits are key responsibilities, so proactive training and fostering a culture of continuous improvement are essential for success in this role.

What is the difference between Associate Director Quality vs Quality Manager?

AspectAssociate Director QualityQuality Manager
ResponsibilitiesOversees quality strategies, compliance, and cross-departmental initiatives at a higher levelManages daily quality operations, audits, and team supervision
Required CredentialsTypically requires advanced degrees and extensive experience in quality assuranceRequires relevant certifications and experience in quality management
Work EnvironmentStrategic, cross-functional, often involved in policy developmentOperational, focused on process implementation and team management

The Associate Director Quality generally holds a higher strategic role with broader responsibilities compared to the more operational focus of a Quality Manager. While both roles require relevant credentials and experience, the Associate Director is involved in shaping quality policies and ensuring compliance at an organizational level, whereas the Quality Manager oversees daily quality activities and team performance.

What are popular job titles related to Associate Director Quality jobs in Raleigh, NC?

For Associate Director Quality jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Associate Director Quality jobs in Raleigh, NC look for?

The top searched job categories for Associate Director Quality jobs in Raleigh, NC are:

Associate Director Quality jobs near you
Infographic showing various Associate Director Quality job openings in Raleigh, NC as of September 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% In-person job distribution, with an average salary of $54,454 per year, or $26.2 per hour.

QA Operations Head (Associate Director)

Durham, NC • On-site

Novartis Pharmaceuticals Corporation
10K+ employees
Learn more about Novartis Pharmaceuticals Corporationexternal

$138K - $257K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 23 days ago

Key responsibilities

  • Lead Quality Operations oversight to ensure compliance across manufacturing activities and QA Operational Excellence.

  • Provide quality leadership for product release, batch record review, and disposition activities.

  • Lead continuous improvement initiatives to strengthen quality performance, compliance, and operational excellence.

Job description

Band

Level 5


Job Description Summary

Join Novartis as our QA Operations Head and play a pivotal role in ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity to lead a critical Quality Operations organization at our new small molecule manufacturing site in Morrisville, partnering closely with Manufacturing, Quality Control, and technical teams to drive operational excellence, product quality, and regulatory compliance. As a visible site leader, you will empower and develop high-performing teams, champion continuous improvement, and help shape the future of quality within a dynamic and growing manufacturing environment.


Job Description

Key Responsibilities

  • Lead Quality Operations oversight to ensure compliance across manufacturing activities and QA Operational Excellence.
  • Provide quality leadership for product release, batch record review, and disposition activities.
  • Drive investigation of deviations, out-of-expectation results, and complaints, ensuring effective corrective actions.
  • Lead continuous improvement initiatives to strengthen quality performance, compliance, and operational excellence.
  • Support validation, technology transfer, commissioning, and implementation of new manufacturing processes and equipment.
  • Ensure ongoing inspection readiness and successfully support internal, customer, and regulatory audits and inspections.
  • Develop, coach, and lead high-performing teams while fostering a culture of accountability and learning.
  • Manage resources, capacity planning, and quality metrics to achieve business and compliance objectives.
  • Explore the potential of data and technology to support the manufacturing site's transformation journey in line with Novartis Technical Operations strategy.

Essential Requirements

  • Bachelor of Science or Master of Science in Life Sciences, Pharmacy, Chemistry, Biotechnology, or related scientific discipline; advanced degree preferred.
  • Minimum 8-10 years of relevant pharmaceutical experience including direct experience in oral solid dosage manufacturing which can include expert roles in Production, Manufacturing Science and Technology and/or Engineering, in addition to Quality.
  • Demonstrated Quality Operations leadership experience with responsibility for product release, compliance, inspection readiness, people leadership, talent development, performance management, and cross-functional collaboration.
  • Experience with Heath Authority inspections (preferably FDA) and regulatory procedures
  • Proven experience leading deviation investigations, corrective and preventive actions, validation activities, and continuous improvement initiatives.

Desirable Requirements

  • Previous involvement with facility start-ups, qualifications, validations, transfers
  • Qualifications or certification in Lean Management, Operational Excellence, or continuous improvement methodologies.

The salary for this position is expected to range between $138,600 and $257,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

#LI-Onsite


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$138,600.00 - $257,400.00


Skills Desired

Collaboration, Data Integrity, Decision Making, Leadership

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