Sr. Automation Engineer – DeltaV

Novartis AG; Durham (NC); On-site; USD 109,000 - 202,000; Full time

Benefits offered by this job

Health benefits

401(k) with company match

Generous time off

Job summary

Novartis in Durham, NC is seeking a Sr. Automation Engineer – DeltaV to lead automation initiatives within a GMP manufacturing environment. You will serve as a technical expert, design, configure, and optimize DeltaV control strategies, and drive the full automation lifecycle from implementation to handover.

Collaborate with Manufacturing, Engineering, Quality, Validation and IT to deliver reliable solutions that improve product quality and compliance with GMP and FDA 21 CFR Part 11.

Qualifications

• Bachelor's degree in Engineering or related field with 8+ years GMP pharma experience.
• Hands-on DeltaV DCS programming, troubleshooting, and maintenance.
• Experience with regulated environments (FDA 21 CFR Part 11) and lifecycle validation.

Responsibilities

• Serve as a DeltaV SME for GMP manufacturing automation.
• Design, configure, troubleshoot DeltaV control strategies.
• Lead automation projects from concept to handover.
• Collaborate with Manufacturing, Quality, Validation, IT.
• Drive continuous improvement for reliability and quality.
• Ensure GMP, FDA, and data integrity compliance.

Skills

DeltaV DCS

GMP manufacturing

Automation systems

SCADA/HMI/PLC

DeltaV programming

Validation

CAPA

Cross-functional

Documentation

Regulatory compliance

Education

Bachelor's degree in Engineering

Tools

DeltaV

HMI software

BMS

Job description

Job Description Summary

Join Novartis and play a pivotal role in advancing manufacturing automation that helps deliver innovative medicines to patients worldwide. As a Sr. Automation Engineer – DeltaV, you will serve as a key technical expert supporting and optimizing critical automation systems within a GMP-regulated manufacturing environment. This is an opportunity to lead impactful automation initiatives, drive system reliability and performance, and collaborate with cross-functional teams to enable operational excellence. If you're passionate about automation, continuous improvement, and leveraging DeltaV technology to solve complex challenges, we'd love to hear from you.

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

• Serve as a DeltaV SME, providing technical expertise for automation systems supporting GMP manufacturing operations.
• Design, configure, troubleshoot, and optimize DeltaV control strategies and system performance.
• Support the full automation system lifecycle, including implementation, upgrades, maintenance, and retirement.
• Lead automation projects from concept through commissioning, qualification, and operational handover.
• Partner with Manufacturing, Engineering, Quality, Validation, and IT teams to deliver automation solutions.
• Drive continuous improvement initiatives to enhance system reliability, efficiency, and product quality.
• Investigate automation deviations, implement corrective actions, and support CAPA activities.
• Develop and maintain automation documentation, including specifications, test protocols, and system drawings.
• Ensure automation systems remain compliant with GMP, FDA, and data integrity requirements.
• Provide technical mentorship and subject matter expertise for DeltaV and site automation technologies.

Essential Requirements

• Bachelor's degree in Engineering, Computer Science, Automation, or a related technical field with 8+ years of experience supporting GMP pharmaceutical or biopharmaceutical manufacturing operations; or equivalent experience.
• Strong hands-on experience programming, troubleshooting, and maintaining DeltaV DCS automation systems.
• Experience supporting SCADA, HMI, PLC, BMS, and manufacturing automation platforms in a regulated environment.
• Demonstrated knowledge of GMP, FDA, and 21 CFR Part 11 requirements supporting manufacturing automation systems.
• Experience with automation system validation, qualification, and lifecycle management within GMP operations.
• Proven ability to lead automation projects, execute complex change controls, and drive continuous improvement initiatives.
• Experience developing automation documentation, technical specifications, and test protocols.
• Strong communication and collaboration skills with experience partnering across Engineering, Manufacturing, Quality, Validation, and IT teams.

Novartis Compensation and Benefit Summary

The salary for this position is expected to range between $108,500 and $201,500 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.

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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 [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.

Salary Range

$108,500.00 - $201,500.00

Skills Desired

• Business Continuity
• Cost Management
• Data Analytics
• Decision Making
• Emotional Resilience
• Engineering Concepts
• Good Documentation Practices
• Health, Safety, and Environment (HSE) Policy
• Manufacturing Processes
• Operational Excellence
• Operations Management
• Planning Budgeting And Forecasting (PBF)
• Problem Solving
• Project Management
• Quality Compliance
• Risk Management
• Stakeholder Management
• Vendor Management