Principal Engineer, MS&T

Drive the future of gene therapy manufacturing and make a meaningful impact on patients’ lives. As a Principal Engineer, MS&T, you will serve as a scientific and technical leader for upstream processes, bringing deep expertise in gene therapy manufacturing to support innovation, troubleshoot complex challenges, and continuously elevate product quality. You will play a critical role in shaping manufacturing excellence, leading cross-functional collaboration, and advancing cutting-edge technologies to ensure reliable, high-quality delivery of life-changing therapies.

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: Provide technical leadership and subject matter expertise for complex scientific investigations, regulatory submissions, and inspectionsLead the analysis of process verification and manufacturing data to identify trends, assess process performance, and drive data driven continuous improvement initiativesLeverage deep expertise in upstream manufacturing processes (including mammalian cell culture and gene therapy platforms) to troubleshoot and resolve complex manufacturing issues across internal operations and external partners (CMOs)Mentor and develop MS&T staff, providing technical guidance in upstream processing, including troubleshooting of complex platforms such as triple transfectionLead and support product technology transfers into GMP manufacturing environments, ensuring successful scale-up, process robustness, and knowledge transfer across receiving sitesPartner cross-functionally with Manufacturing, Quality, Engineering, and Validation teams to ensure reliable execution of production processes and sustained commercial supplyMonitor critical quality attributes and process parameters to maintain product consistencyDefine and implement process improvements with global process owners and operations teamsSupport the startup, qualification, and lifecycle management of manufacturing equipment, systems, and processes, ensuring compliance with validation and regulatory expectationsAuthor, review, and approve technical documentation (e.g., investigations, change controls, process descriptions) to ensure accuracy, completeness, and regulatory defensibilityDrive operational excellence initiatives and collaborate with Quality to ensure regulatory complianceEssential Requirements: Bachelor’s degree with at least 12 years, Master’s degree with 10 years, or PhD with at least 8 years of relevant experience. OR 9 years of experience with 3 + years of Novartis gene therapy process support.  Experience in biopharmaceutical manufacturing aligned with the degree and years of experience outlined aboveStrong expertise in mammalian cell culture and bioreactor systems, both suspension and adherentDemonstrated experience with upstream processing, including triple transfection for gene therapyDeep understanding of GMP requirements and validation principlesProven ability to lead complex technical troubleshooting and manufacturing investigationsStrong written and verbal communication skills across cross-functional teamsExperience with technology transfer, process improvement, and operational excellence initiativesNovartis Compensation and Benefit Summary:The salary for this position is expected to range between $126,000 and $234,000 annuallyThe 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