QA Compliance Specialist

Job Description Summary In this role, you'll be at the heart of ensuring quality, compliance, and trust as we advance innovative gene therapies for patients worldwide. As a QA Compliance Specialist, your expertise will directly shape how quality systems are applied, strengthened, and continuously improved across the site—supporting both development and commercialization. You'll partner closely with cross-functional teams, influence critical decisions, and serve as a trusted voice on compliance, helping turn complex challenges into clear, risk-based solutions that protect patients and products alike.

Job Description Location:

This position will be located in Durham, NC and will be a Hybrid role. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

Establish and maintain site quality system processes supporting development and commercialization of advanced gene therapy medicines Drive consistent execution of change control and non-conformance programs aligned with global quality system standards Lead investigations, root cause analysis, and timely corrective and preventive actions using a risk-based approach Serve as subject matter expert for change control, non-conformance, and quality documentation programs Lead non-conformance and change control review board meetings, ensuring effective governance and decision-making Review, approve, and author standard operating procedures to ensure regulatory and quality system compliance Analyze quality system metrics, trend performance, and present actionable insights to drive continuous improvement Provide guidance and training to site users on quality system processes and expectations Partner with manufacturing and operations on product investigations, deviations, and compliance activities Ensure adherence to Good Manufacturing Practice requirements and support inspection readiness across the site

Essential Requirements:

Bachelor's degree in life sciences, chemistry, or related field, with significant experience in regulated manufacturing environments Proven experience in Quality Assurance within pharmaceutical, biotechnology, or gene therapy manufacturing Strong working knowledge of quality systems, including change control, non-conformance management, and deviation handling Demonstrated experience applying data integrity principles and ensuring compliance with current regulatory expectations Hands-on experience supporting Good Manufacturing Practice operations through quality management system execution Solid understanding of regulatory guidelines and expectations from global health authorities Experience reviewing, authoring, and approving standard operating procedures and quality documentation Ability to work independently, manage multiple priorities, and communicate clearly across technical and operational teams

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $81,200 and $150,800 annually 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. #

LI-Hybrid 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, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. 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 to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or 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. Salary Range $81,200.00 - $150,800.00 Skills Desired Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Problem Solving Skills, Project Management, Regulatory Requirements knowledge, Risk Management Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people's lives. Novartis is aware of employment scams which make false use of our company name or leader's names or recruiter's names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .