Validation Lead

Job Overview Band Level 4 Job Description Summary. Location: Morrisville, North Carolina. Join Novartis and play a pivotal role in shaping the future of pharmaceutical manufacturing at our growing Morrisville site. As the Validation Lead, you will drive the site’s validation strategy across process, cleaning, packaging, and ongoing verification activities, ensuring products are delivered with the highest standards of quality, compliance, and patient safety. This is a unique opportunity to build and influence validation programs from the ground up, partner with cross‑functional experts, and contribute directly to successful product launches, technical transfers, and regulatory readiness in a dynamic and innovative manufacturing environment. Key Responsibilities Lead the site validation strategy across process, cleaning, packaging, and ongoing process and cleaning verification activities. Own and maintain the Validation Master Plan, ensuring timely execution and inspection readiness. Establish, monitor, and improve validation performance metrics to support compliance and operational excellence. Provide technical leadership for validation risk assessments, investigations, and complex validation challenges. Partner with Engineering, Quality, Analytical Science & Technology, and IT to define interfaces to equipment qualification / utilities qualification, system qualification, and analytical method validation. Support product launches and technical transfers by defining robust validation approaches and delivering required data. Represent the site during audits, inspections, and validation governance activities while maintaining compliance standards. Essential Requirements Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or a related scientific discipline. 8 years of experience in manufacturing / manufacturing science and technology / technical development / quality in oral solid dosage pharmaceutical manufacturing. 5 years of experience executing process validation, including experience leading and managing validation projects. Proven expertise leading process validation, cleaning validation, and ongoing process verification programs. Strong knowledge of quality systems, applied statistics, and global regulatory requirements. Demonstrated success managing complex cross‑functional projects and authoring technical validation documentation. Desirable Requirements PhD in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or equivalent. Experience with change controls, data analytics, GMP, quality compliance, and regulatory compliance. Leadership experience in technology transfer and process improvement. Compensation and Benefits The salary for this position is expected to range between $126,000 and $234,000 per year. The final salary offered is determined based on relevant skills and experience and updated periodically. Salary is complemented by performance‑based cash incentive and, depending on the level of the role, eligibility for annual equity awards. US‑based eligible employees 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. Employees also receive a generous time‑off package, including vacation, personal days, holidays, and other leaves. EEO Statement The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, or promotion based on 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 you need a reasonable accommodation for any part of the application process or to perform essential functions of this position, please email View email address on click.appcast.io or call View phone number on click.appcast.io and include the job requisition number. #J-18808-Ljbffr