Technical Steward

U473 (FCRS = US473) Novartis Innovative Technologies Inc; Morrisville (NC); On-site; USD 126,000 - 234,000; Full time

Benefits offered by this job

Health, life & disability benefits

401(k) with company match

generous paid time off

Job summary

Novartis Innovative Technologies Inc. in Morrisville, North Carolina is seeking a Technical Steward to drive advanced manufacturing technologies, process excellence, and global collaboration across manufacturing operations.

You will lead process development, qualification, validation, and capital project activities, partnering with MS&T teams to implement new standards and innovations. Strong communication and data-driven problem solving are essential.

Qualifications

• Bachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or a related scientific discipline.
• Minimum five years of experience in oral solid dosage pharmaceutical manufacturing.
• Strong understanding of pharmaceutical manufacturing processes, regulatory requirements, and GMP.
• Experience supporting process improvement, technology transfer, validation, or manufacturing science activities.
• Ability to investigate technical issues, analyze data, and implement effective process solutions.
• Effective communication and collaboration skills with the ability to influence cross-functional stakeholders.

Responsibilities

• Act as the single point of contact (SPOC) for the interface with global MS&T network and with technical development organization, for the corresponding global activities, to define and implement new technical standards for existing and new technologies and equipment.
• Serve as the site subject matter expert for specific pharmaceutical manufacturing process technologies, locally, including any pilot scale, scale up or down, and Design of Experiments (DoE).
• Partner with global and development teams to implement new technical standards and manufacturing innovations.
• Lead process optimization initiatives to improve robustness, efficiency, yield, and operational performance.
• Provide technical expertise for equipment selection, qualification, validation, and capital project activities.
• Support technology transfers, process scale-up activities, and commercial manufacturing readiness.
• Drive technical investigations, risk assessments, and root cause analysis for manufacturing challenges.
• Deliver technical training and share knowledge to strengthen site and network capabilities.

Skills

Process optimization

Cross-functional collaboration

Data analysis

Education

Bachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or related scientific discipline

Master of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or related scientific discipline

Job description

Job Description Summary

Location: Morrisville, North Carolina Imagine shaping the future of pharmaceutical manufacturing through scientific expertise, innovation, and global collaboration. As a Technical Steward at Novartis, you will serve as a trusted subject matter expert supporting advanced manufacturing technologies and processes that deliver high-quality medicines to patients worldwide. Working at the intersection of science, technology, and operations, you will drive process excellence, influence the implementation of new technologies, partner with global experts, and help build a culture of continuous improvement at our Morrisville site. This is an exciting opportunity to make a meaningful impact while growing your technical leadership within a world-class manufacturing organization.

Key Responsibilities

• Act as the single point of contact (SPOC) for the interface with global MS&T network and with technical development organization, for the corresponding global activities, to define and implement new technical standards for existing and new technologies and equipment.
• Serve as the site subject matter expert for specific pharmaceutical manufacturing process technologies, locally, including any pilot scale, scale up or down, and Design of Experiments (DoE).
• Partner with global and development teams to implement new technical standards and manufacturing innovations.
• Lead process optimization initiatives to improve robustness, efficiency, yield, and operational performance.
• Provide technical expertise for equipment selection, qualification, validation, and capital project activities.
• Support technology transfers, process scale-up activities, and commercial manufacturing readiness.
• Drive technical investigations, risk assessments, and root cause analysis for manufacturing challenges.
• Deliver technical training and share knowledge to strengthen site and network capabilities.

Essential Requirements

• Bachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or a related scientific discipline.
• Minimum five years of experience in oral solid dosage pharmaceutical manufacturing.
• Strong understanding of pharmaceutical manufacturing processes, regulatory requirements, and GMP.
• Experience supporting process improvement, technology transfer, validation, or manufacturing science activities.
• Ability to investigate technical issues, analyze data, and implement effective process solutions.
• Effective communication and collaboration skills with the ability to influence cross-functional stakeholders.

Desirable Requirements

• Master of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or a related scientific discipline.
• Experience presenting technical findings, publishing scientific work, or participating in industry conferences.

Salary

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 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.

Salary Range $126,000.00 - $234,000.00

Benefits

• 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.

EEO Statement

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 [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Additional Information

To learn more about the culture, rewards and benefits we offer our people click here. #LI-Onsite

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