Are you an experienced IT Automation Engineer who wants to be part of building automated manufacturing solutions for medical device production, changing the lives for millions of patients, this could be your next challenge…


The position

The IT Automation Engineer position involves designing and implementing efficient and reliable IT Automation solutions for a highly automated production facility. The Engineer will be responsible for connecting production equipment such as PLCs/HMIs and material handling systems such as cranes, AGVs, and conveyors to SCADA and MES (PAS-X). They will also enable automated data collection, support batch documentation, and continuously improve the automation systems.


As an IT Automation Engineer, you will:

Be responsible for designing and implementing robust and efficient IT/Automation solutions, connecting Production Equipment (PLC’s/HMI) and material handling systems (Cranes/AGV’s/Conveyors) to SCADA and MES (PAS-X).
Enable automated Data Collection, supporting batch documentation and continuous improvements in a highly automated production facility.
Work closely with tracks leads, external partners and internal stakeholders within the different IT/Automation teams across our entire organization.
Participate in Test/Validation and documentation of the implemented IT/automation solutions.
Ensure a high operating efficiency and later being part of the operation & maintenance organization.
The successful completion of this project will position Novo Nordisk as a leader in pharmaceutical manufacturing and strengthen its position in the competitive global market. The IT Automation Engineer's contribution to the project will be crucial in ensuring its success and will have a significant impact on the organization's achievements and future growth.


Qualifications


To succeed in this role, we expect you to have:

A degree within automation engineering/computer science or equivalent combination of experience & education.
Minimum 3 years of experience within IT/Automation engineering, preferably within the Pharmaceutical (cGMP/GxP) or other regulated industry, incl. documentation and testing of IT/Automation solutions and related interfaces (PLC/SCADA/MES).
Strong communication/collaboration skills with internal & external stakeholders, incl. system suppliers, end-users, project managers, etc.
Good communication skills (written & verbally) in English.