Novartis

pharmaceutical

AutomationEngineer

$99–99k Durham, North Carolina, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Automation Engineer at Novartis. Skills: GMP automation systems, Distributed Control Systems, Supervisory Control and Data Acquisition, Human Machine Interface platforms, Programmable Logic Controllers, Building systems, Data historians, System validation, Change control. Own and maintain building management and environmental monitoring systems supporting a new manufacturing facility. Design, configure, install, and maintain automation software and associated hardware across GMP and non-GMP syst”

What You'll Achieve.

ensure safe, reliable medicines reach patients; shape how advanced automation supports quality, compliance, and operational excellence; enable a compliant and efficient production environment; seeing the direct results of your expertise in a highly regulated setting; support a compliant, inspection-ready manufacturing environment

Industry & Context.

pharmaceutical
Problems you'll solve

solving complex problems; Troubleshoot and resolve automation-related issues

Eligibility Requirements

onsite role, Novartis is unable to offer relocation support for this role

What They're Looking For.

Must Have

Bachelor’s degree in Engineering, Computer Science, or a related technical discipline, Minimum five years of experience supporting GMP automation systems in pharmaceutical or biopharmaceutical manufacturing environments, Hands-on experience with Distributed Control Systems, including Emerson DeltaV, Experience with Supervisory Control and Data Acquisition and Human Machine Interface platforms, including Copadata enon and Rockwell FactoryTalk, Practical expertise with Programmable Logic Controllers and building systems, including Emerson PACSystems and Allen‑Bradley CompactLogix and ControlLogix, Working knowledge of data historians and manufacturing data systems, including OSIsoft PI, and basic Structured Query Language query development, Demonstrated understanding of system validation, change control, and regulated automated manufacturing environments

Nice to Have

Knowledge Of Relevant Tools And Systems, Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance

What You'll Do.

Own and maintain building management and environmental monitoring systems supporting a new manufacturing facility

and maintain automation software and associated hardware across GMP and non-GMP systems

Lead integration of third-party equipment into plant automation and distributed control systems

Prepare scopes of work and manage automation contractors to meet project timelines and quality expectations

Develop project objectives aligned with user requirements

and operational priorities

Author and maintain system documentation

including user requirements and functional specifications

Ensure automation systems meet GMP

and internal compliance requirements

Partner with Quality to support a compliant

inspection-ready manufacturing environment

Troubleshoot and resolve automation-related issues impacting operations and production performance

Execute change controls and support investigations related to automation system non-conformances

How You'll Work.

Team & Collaboration

Partnering with engineering, quality, and manufacturing teams; communication and collaboration skills when working across engineering, quality, and operations teams

Communication Scope

communication and collaboration skills

Process & Methodology

Prepare scopes of work, manage automation contractors to meet project timelines and quality expectations, Develop project objectives aligned with user requirements, business plans, and operational priorities

Full Job Description

**Band** Level 3 **Job Description Summary** At Novartis, automation is more than technology — it is how we ensure safe, reliable medicines reach patients. In this role, you will take ownership of critical building management and environmental monitoring systems within a new manufacturing facility, helping shape how advanced automation supports quality, compliance, and operational excellence. You will work at the intersection of innovation and impact, partnering with engineering, quality, and manufacturing teams to design, maintain, and continuously improve systems that enable a compliant and efficient production environment. If you enjoy solving complex problems, influencing how manufacturing systems perform at scale, and seeing the direct results of your expertise in a highly regulated setting, this role offers meaningful responsibility and long-term growth. **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:** * Own and maintain building management and environmental monitoring systems supporting a new manufacturing facility * Design, configure, install, and maintain automation software and associated hardware across GMP and non-GMP systems * Lead integration of third-party equipment into plant automation and distributed control systems * Prepare scopes of work and manage automation contractors to meet project timelines and quality expectations * Develop project objectives aligned with user requirements, business plans, and operational priorities * Author and maintain system documentation, including user requirements and functional specifications * Ensure automation systems meet GMP, regulatory, and internal compliance requirements * Partner with Quality to support a compliant, inspection-ready manufacturing environment * Troubleshoot and resolve automation-related

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