Automation Engineer

III - BMS/PLC/OEM

Novartis - 4.1 Durham, NC Job Details Full-time $98,700 - $183,300 a year 1 day ago Benefits Health insurance 401(k) matching Qualifications Systems architecture experience within technology

FDA 21 CFR

Part 11 GMP Industrial equipment troubleshooting Production validation processes Regulatory/legal compliance standards in production Supervisory control and data acquisition (SCADA) Cross-functional communication Production troubleshooting Full Job Description Summary Imagine being the automation expert who helps keep critical manufacturing systems running seamlessly while supporting the production of medicines that impact patients around the world. As an Automation Engineer III focused on BMS, PLC, and OEM systems, you'll play a key role in maintaining and enhancing complex manufacturing automation platforms, partnering across Engineering, Manufacturing, and Quality teams to deliver reliable, compliant, and efficient operations. This is an opportunity to apply your technical expertise across GMP manufacturing systems, drive continuous improvement initiatives, and influence projects that support current operations as well as future manufacturing capabilities. About the

Role 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:

Maintain, troubleshoot, and optimize BMS, PLC, OEM, and other manufacturing automation systems. Support design, configuration, installation, and lifecycle management of automation hardware and software. Integrate OEM and third-party equipment with site DCS, BMS, and manufacturing systems. Lead automation activities for capital projects, upgrades, and system enhancements. Develop URS, FS, DDS, HDS, and SDS documentation for automation solutions. Execute and support change controls, validation activities, and regulatory compliance initiatives. Partner with Manufacturing and Quality teams to resolve complex production issues. Support GMP manufacturing operations through on-call and operational support activities. Drive continuous improvement projects that enhance reliability, compliance, and operational efficiency. Maintain automation procedures, SOPs, and system records in alignment with FDA and GMP requirements.

Essential Requirements:

Bachelor's degree in Engineering, Computer Science, or a related technical field. Minimum 5 years of experience in pharmaceutical or biopharmaceutical GMP manufacturing operations, or 9 years of equivalent industry experience. Hands-on experience programming, troubleshooting, and maintaining DCS platforms, preferably DeltaV. Experience supporting PLC, BMS, and

SCADA/HMI

systems in a regulated manufacturing environment. Knowledge of automation validation, change controls, and

FDA 21 CFR

Part 11 requirements. Experience with data historian technologies, preferably OSI PI. Strong understanding of industrial communication protocols, instrumentation, and control system architecture. Excellent communication and collaboration skills with the ability to work across technical and business teams.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $98,700 and $183,300 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. #

LI-Onsite Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?

https:

//www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

Learn about all the ways we'll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

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 & 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 [email protected] 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. Division Operations Business Unit Information Technology Location USA State North Carolina Site Durham Company / Legal Entity U061 (FCRS = US061) Novartis Services, Inc. Functional Area Technical Operations Job Type Full time Employment Type Regular Shift Work No