Sr. Engineer, MS&T - Aseptic Drug Product

Novartis AG; North Carolina; On-site; USD 114,000 - 212,000; Full time

Job summary

Novartis in Durham, NC is seeking a Sr. Engineer, Manufacturing Science and Technology – Aseptic Drug Product, onsite to lead process improvements and technical investigations.

You will partner with Manufacturing, Quality, Engineering, and global teams to ensure reliable supply of high-quality sterile products, driving CPV, tech transfer, validation, and lifecycle management with a focus on continuous improvement.

Qualifications

• Bachelor’s degree in Biochemistry, Chemical Engineering, Bioengineering, or related technical field with 6+ years of biopharmaceutical manufacturing experience; Master’s degree with 4+ years; or Doctorate with 2+ years.
• Proven experience in GMP biopharmaceutical manufacturing operations.
• Hands-on aseptic fill-finish and sterile drug product manufacturing experience.

Responsibilities

• Lead CPV activities by analyzing process data and driving performance improvements.
• Serve as MS&T technical lead for investigations, root cause analysis, and issue resolution.
• Support production schedules, commercial supply, and GMP compliance.
• Monitor CQAs and CPPs to ensure product quality and process control.
• Identify and implement process improvements to enhance reliability and efficiency.
• Support new equipment, systems, and manufacturing process startups.

Skills

Analytical skills

Data-driven decisions

Cross-functional collaboration

Process data interpretation

Education

Bachelor's degree in Biochemistry, Chemical Engineering, Bioengineering, or related field

Master's degree (4+ years experience)

Doctorate (2+ years experience)

Tools

GMP regulations

Process validation

Lifecycle management

Job description

Job Description Summary

Imagine being at the forefront of delivering life-changing sterile medicines to patients around the world. As Sr. Engineer, Manufacturing Science and Technology - Aseptic Drug Product, you will play a critical role in advancing aseptic manufacturing operations by providing technical leadership, driving process performance, and supporting the successful introduction of new products and technologies. Working closely with Manufacturing, Quality, Engineering, and global partners, you will help solve complex challenges, lead continuous improvement initiatives, and ensure a reliable supply of high-quality products for patients. This is an exciting opportunity to make a meaningful impact in a collaborative environment that values innovation, scientific excellence, and operational excellence.

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 CPV activities by analyzing process data, identifying trends, and driving process performance improvements.
• Serve as the MS&T technical lead for manufacturing investigations, root cause analysis, and issue resolution.
• Partner with Manufacturing to support production schedules, commercial supply, and compliance with GMP requirements.
• Monitor and trend CQAs and CPPs to ensure consistent product quality and process control.
• Identify, evaluate, and implement process improvements that enhance reliability, efficiency, and performance.
• Support the introduction of new equipment, systems, and manufacturing processes through startup and implementation activities.
• Author and support process change documentation while collaborating with Engineering, Manufacturing, and Validation teams.
• Provide technical expertise for remediation efforts, project deliverables, technical assessments, and process reports.
• Collaborate with Development and site partners to execute Tech Transfer activities and ensure successful product commercialization.
• Drive OPEX initiatives and foster a culture of continuous improvement, quality, and manufacturing excellence.

Essential Requirements

• Bachelor's degree in Biochemistry, Chemical Engineering, Bioengineering, or a related technical field with 6+ years of biopharmaceutical manufacturing experience; Master's degree with 4+ years of experience; or Doctorate degree with 2+ years of experience.
• Proven experience supporting GMP biopharmaceutical manufacturing operations within a regulated environment.
• Hands-on experience with aseptic fill-finish operations and sterile drug product manufacturing.
• Experience supporting Tech Transfer, process validation, lifecycle management, or manufacturing process improvements.
• Working knowledge of global GMP regulations, validation requirements, and quality compliance expectations.
• Strong analytical skills with the ability to interpret process data, identify trends, and drive data-based decisions.
• Excellent technical writing, communication, and cross-functional collaboration skills.
• Demonstrated ability to lead technical initiatives and contribute effectively within cross-functional teams.

Novartis Compensation and Benefit Summary

The salary for this position is expected to range between $114,100 and $211,900 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.

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 req