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Senior Engineer, MS&T
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U473 (FCRS = US473) Novartis Gene Therapies
Durham, NC (In Person)
$163,000 Salary, Full-Time
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Job Description
Step into a high-impact role where your expertise will directly shape the delivery of life-saving therapies. As a key member of Manufacturing Science and Technology, you'll lead process improvements and drive innovation in sterile drug product manufacturing, partnering cross-functionally to ensure quality, efficiency, and reliability. This is your opportunity to solve complex challenges, influence production outcomes, and play a critical role in bringing medicines to patients.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
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
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 process investigations to resolve manufacturing issues and drive continuous improvementsAnalyze process verification data to identify trends and ensure consistent product qualityPartner with manufacturing to meet production schedules and maintain reliable drug supplyMonitor critical quality attributes and process parameters to control variability and driftImplement process improvements in collaboration with operations and engineering teamsSupport startup and qualification of new equipment, systems, and manufacturing processesDocument and manage updates to manufacturing processes in compliance with quality standardsProvide technical expertise for projects, including remediation and process enhancement initiativesSupport technology transfer to ensure seamless transition into compliant GMP manufacturingCollaborate with Quality to maintain a compliant and inspection-ready production environmentEssential Requirements:
Bachelor of Science degree with 6 years, Master of Science with 4 years, or PhD with 2 years of biopharmaceutical manufacturing experienceStrong experience supporting GMP drug product manufacturing environments, including aseptic processing and fill/finish operationsProven ability to analyze data and apply scientific principles to solve complex process issuesExcellent written and verbal communication skills with strong technical writing capabilityDemonstrated ability to collaborate effectively across cross-functional teamsFamiliarity with global regulatory requirements for drug products, validation, and qualificationAbility to manage multiple priorities and contribute to continuous improvement initiativesNovartis Compensation and Benefit Summary:
The salary for this position is expected to range between $114,100 to $211,900 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