Automation Engineer I/II - DeltaV

BioSpace; Clayton (NC); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Performance bonus

Paid time off 14 holidays

Health insurance

Dental insurance

Vision insurance

401K match

Parental leave

Family medical leave

Product access

Tuition assistance

Life insurance

Disability insurance

Referral rewards

Job summary

Novo Nordisk is seeking an Automation/Process Control Engineer to drive alignment of control systems with local and global standards at the Clayton API facility. You will work with stakeholders and vendors to ensure equipment IFA specs and connection readiness for manufacturing.

The role emphasizes governance, continuous improvement, audits, and project execution using cLEAN/Six Sigma methodologies while maintaining a strong safety and quality mindset.

Qualifications

• Bachelor's degree in engineering or related field from an accredited university.
• Associate’s degree in engineering with 5 years of engineering experience in process-based manufacturing.
• High School/GED with 7 years of engineering experience in process-based manufacturing.
• Minimum of 3 years engineering experience in process-based manufacturing.

Responsibilities

• Support plans to maintain and improve process control systems.
• Coordinate with manufacturing schedules and project plans.
• Serve as automation resource on projects involving process control systems.
• Adhere to automation standards and update related specifications and maintenance plans.
• Support audits and inspections for process control systems.
• Apply cLEAN/Six Sigma problem solving in projects.

Skills

Team collaboration

Cross-functional communication

Problem solving

Project management

Education

Bachelor's degree in engineering

Associate degree in engineering

High school diploma with 7 years engineering experience

Tools

SAP EM

PLC

DCS/SCADA

MES

Oracle

MS SQL

Historian

SAP EWM

Job description

About The Department

At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the‑art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk’s innovative oral products. At API, you’ll join a global network of manufacturing professionals who are passionate about what they do.

What We Offer You

• Leading pay and annual performance bonus for all positions
• All employees enjoy generous paid time off including 14 paid holidays
• Health Insurance, Dental Insurance, Vision Insurance – effective day one
• Guaranteed 8% 401K contribution plus individual company match option
• Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
• Free access to Novo Nordisk-marketed pharmaceutical products
• Tuition Assistance
• Life & Disability Insurance
• Employee Referral Awards

The Position

Work with business stakeholders and/or project team and vendors to ensure process control systems for existing and/or new equipment and processes are in alignment with local and global standards. Work with equipment vendors to spec equipment IFA's and requirements ensuring the equipment is ability to connect to and be used in local manufacturing meeting all requirements through people & equipment focus, as well as serving as gatekeeper for standards.

Relationships

Reports to Manager, Senior Manager.

Essential Functions

• Support plans to maintain & improve process control systems
• Schedule & execute plans in coordination with manufacturing schedules
• Operate as automation resource on projects that involve process control systems
• Own self-development & initiative to understand the site process control systems
• Adhere to the automation standards & implement the necessary changes to the automation-related specifications & maintenance plans
• Support audits & inspections for process control systems
• Utilize the appropriate cLEAN® tools within the main areas of Systematic Problem Solving, process improvement, & project management
• Operate within compliance with a Quality Mindset that focuses on risk management & mitigation
• Implement effective change management
• Support Corporate, PS, local IT, & local stakeholder initiatives & projects
• Participate in the development of new SOPs, best practices and maintenance procedures
• Follow all safety & environmental requirements in the performance of duties

Other Accountabilities, As Assigned

Physical Requirements

Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time.

Qualifications

• Bachelor's Degree in engineering or related field of study from an accredited university required:
• May consider an Associate’s degree in engineering or related field from an accredited university with a minimum of five (5) years of engineering experience in process-based manufacturing, utility, &/or packaging systems required
• May consider a High School Degree/GED with a minimum of seven (7) years of engineering experience in process-based manufacturing, utility, &/or packaging systems required
• Minimum of three (3) years engineering experience in process-based manufacturing, utility, &/or packaging systems required
• For Logistics roles only: Warehouse automation equipment a plus (Automated storage and Retrieval Systems, Automated Guided vehicles, Autonomous Mobile Robots and Conveyor systems)
• Knowledgeable in the following technologies: SAP EM, PLC, DCS/SCADA, MES, Oracle, MS SQL (databases), Historian, general controls a plus SAP EWM a plus
• Proven expertise in planning/organization/execution of engineering activities a plus
• Ability to follow-up on results & revising the work plan for moderately complex problems being resolved by cross functional teams a plus
• Ability to translate high level direction into actionable tasks that deliver results using cLEAN® / Six Sigma methodologies a plus

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.