Validation Engineer III

Job Description Summary Step into a role where your expertise directly enables life-changing therapies to reach patients safely and efficiently. As a Validation Engineer III, you will play a critical role in bringing manufacturing systems to lifeleading validation efforts that ensure compliance, quality, and operational excellence in a cutting-edge GMP environment. Your work will help build and sustain the foundation for reliable, high-quality production, making a meaningful impact on patients around the world. Job Description Location: This position will be located in Durham, NC and will be an onsite role. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Key Responsibilities: Lead commissioning, qualification, and validation activities for manufacturing, laboratory, and utility systems Author, execute, and review validation protocols, reports, and standard operating procedures Oversee user requirement specifications, ensuring compliance, quality, and timely document resolution Perform environmental mapping studies and support specialized validation activities Analyze validation data to confirm accuracy, completeness, and regulatory compliance Develop and support validation strategies and timelines for sustained GMP operations Conduct risk and impact assessments to define system boundaries and validation scope Own validation lifecycle documentation, including plans, assessments, and final reports Support computer systems validation activities for global systems and applications Collaborate with cross-functional teams to support audits, inspections, and project execution Essential Requirements: Bachelors or masters degree in engineering or science with five years of relevant pharmaceutical industry experience Proven experience in validation or engineering within a pharmaceutical or biopharmaceutical environment Strong knowledge of GMP requirements and validation lifecycle stages Hands-on experience with installation, operational, and performance qualification activities Familiarity with global regulatory guidelines, including FDA and International Council for Harmonisation standards Experience performing environmental mapping and using validation tools such as Kaye Validator Experience with biosafety cabinet smoke studies Working knowledge of risk-based validation approaches and industry best practices such as ASTM E2500 and GAMP 5 Excellent technical writing, communication, and problem-solving skills with attention to detail Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $ 98,700 and $183,300 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-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, 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 $98,700.00 - $183,300.00 Skills Desired Business Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems , Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance 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 peoples lives. Novartis is aware of employment scams which make false use of our company name or leaders names or recruiters names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. 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