
Automation Engineer
- Bloomington, IN
- Permanent
- Full-time
Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Automation EngineerFacility: Engineering & TechnicalLocation:Bloomington, IN, USAbout the DepartmentAt Novo Nordisk, we want to make a difference. 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.Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility where talented teams work with innovators to help develop, manufacture and supply products to patients around the world.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
- Serve as a subject matter expert (SME) for automation systems used in drug substance manufacturing.
- Provide lifecycle support for DeltaV DCS and PLC-based control systems.
- Troubleshoot, maintain, and improve automation systems to optimize performance and minimize downtime.
- Support the deployment, change control, and validation of automation code in a GMP environment.
- Collaborate with cross-functional teams to implement process improvements and equipment upgrades.
- Ensure all automation activities comply with FDA, cGMP, and GAMP standards.
- Participate in audits, investigations, and change control processes.
- Support selection and integration of automated manufacturing equipment.
- Partner with commissioning and validation teams to meet FDA GMP compliance.
- Draft, revise, and maintain standard operating procedures (SOPs) and controlled documents.
- Participate in the on-call rotation for off-shift automation support.
- Independently analyze data, identify trends, and propose effective solutions.
- Prepare and complete deviation, investigation, and change control documentation.
- Troubleshoot a wide variety of instrumentation and data systems.
- Recommend new technologies and lead automation-driven process improvements.
- Comply with all safety and environmental regulations.
- Perform other duties as assigned.
- Bachelor's degree in Computer Science, Chemical, Mechanical, Electrical Engineering, or related field; OR 8+ years of relevant engineering experience in lieu of a degree
- 2+ years of engineering-related experience
- Strong understanding of process control, instrumentation, and industrial automation
- Hands-on experience with DeltaV DCS and PLC systems
- Experience working in GMP-regulated environments
- Familiarity with S88 batch processing and automation validation practices
- Working knowledge of automation documentation and change management in a pharmaceutical setting