Product Steward
Novartis is hiring a Product Steward. It pays $126k-$234k a year and Level rates it ; you can apply on Novartis.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- Tools and skills the posting cites include Data Analytics, Statistical Analysis and pharmaceutical manufacturing.
- Level classifies it as a senior role.
- Level lists 837 other open roles at Novartis.
AI in this role
Ensure commercial manufacturing lifecycle quality and process control through data analytics and technical expertise at Novartis.
Job Description Summary
Location: Morrisville, North CarolinaAre you passionate about turning data into insights that improve product quality and manufacturing performance? Join Novartis as a Product Steward and become the technical expert responsible for maintaining deep product and process knowledge throughout the commercial lifecycle. In this highly visible role, you will use data analytics, process monitoring, and scientific expertise to ensure products remain in a state of control, drive continuous improvement initiatives, and support robust, reliable manufacturing operations. Working across multiple functions, you will play a key role in product stewardship, process validation, technical investigations, and operational excellence while helping deliver high-quality medicines to patients.
Job Description
Key Responsibilities
- Serve as the product subject matter expert throughout the commercial manufacturing lifecycle.
- Monitor process performance through data trending, statistical analysis, and ongoing product oversight.
- Lead technical investigations and drive effective corrective and preventive actions for process-related issues.
- Maintain product-specific quality risk assessments and support robust process control strategies.
- Ensure products remain in a continued state of validation through ongoing process verification activities.
- Partner with cross-functional teams to deliver process improvements, optimization initiatives, and manufacturing excellence projects.
- Support regulatory readiness, product transfers, and technical change implementation for assigned products.
Essential Requirements
- Bachelor’s degree in Pharmacy, Pharmaceutical Technology, Chemistry, or equivalent scientific degree.
- Minimum five years of experience in Oral Solid Dosage pharmaceutical manufacturing environments.
- Strong understanding of pharmaceutical manufacturing processes, regulatory requirements, and GMPs.
- Experience using data trending, statistical analysis, and process monitoring to drive decision-making.
- Proven ability to investigate process issues, identify root causes, and implement effective corrective actions.
- Demonstrated experience working collaboratively across technical, quality, and manufacturing functions.
Desirable Requirements
- Master of Science degree in Pharmacy, Pharmaceutical Technology, Chemistry, or a related scientific field.
- Experience supporting product transfers, process optimization initiatives, and manufacturing excellence programs.
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. 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.
To learn more about the culture, rewards and benefits we offer our people click here.
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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
$126,000.00 - $234,000.00
Skills Desired
Applied Statistics, Change Controls, Data Analytics and Digital (Inactive), GDP Knowledge (Inactive), Good Manufacturing Practices (GMP), HSE Knowledge (Inactive), Manufacturing Processes, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process and Cleaning Validation (Inactive), Process Control, Quality Compliance, Regulatory Compliance, Resilience and Risk Management (Inactive), Technical Leadership, Technology TransferHow we rate this
Product Steward at Novartis rates 10 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where pharmaceutical manufacturing was part of your work. What did you do?
- Tell me about a project where process validation was part of your work. What did you do?
- Tell me about a project where quality risk assessment was part of your work. What did you do?
- Tell me about a project where technical investigation was part of your work. What did you do?
- Walk me through how you've used Data Analytics in your day-to-day work.
Adapt your resume
- List these exact terms on your resume: Pharmaceutical Manufacturing, Process Validation, Quality Risk Assessment, Technical Investigation, and Data Analytics. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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