Test System Engineer

Would you like to play a key role in ensuring the quality of Devices? Do you want to make a true impact on millions of people living with diabetes worldwide? Are you ready to have a chance to further develop professionally and personally?

Then you might be our Test System Engineer in our Quality Control (QC) Development team in Device Manufacturing Development (DMD). Read on and apply today!
 

The Position

As a Test System Engineer, in our QC Development and Global Support Team, you will have various tasks and responsibilities. This team covers the full range of Novo Nordisk’s medical device and combination products. Another important part of the job is to support the global network of QC Laboratories regarding compliance, so that we always live up to the requirements from the authorities, including updates and implementation of necessary standard operating procedures (SOP’s) and ensuring that we follow the SOP’s covering our functional area. 

The position gives you a great opportunity to utilize and develop skills in close cooperation with external test and equipment suppliers as well as a broad range of internal stakeholders, including colleagues in the department, other global Novo Nordisk sites, other test departments in Research and Development (R&D), Quality Assurance (QA) and projects managers.

The main tasks will be to:
• Be responsible for the implementation of new systems and test methods in the Development Laboratory. 
• Purchase new equipment in compliance with standards and Novo Nordisk’s Quality Management System procedures.
• Play a key role in the qualification of new systems and transfer of equipment and methods to QC Laboratories around the world. 
• Take part in the specification, configuration management and IT setup of test systems and methods. 
• Provide training of test personnel and regular process confirmation.

Qualifications

The qualifications we value include having:
• A bachelor’s or master’s degree in mechanical engineering or similar. 
• Strong experience with test or production equipment, writing and reviewing scientific documents, with focus on high technical complexity. 
• Familiarity with GMP and LEAN tools. 
• Knowledge of equipment specification, qualification and operating/maintaining of IT systems.
• Fluency in written and spoken English.

On a personal level, you demonstrate solid interpersonal and communication skills. While having a proactive mindset, you enjoy building relationships and collaborating across interdisciplinary boundaries. 

Having the skills to support and motivate others to deliver on their targets is crucial in this position. We will welcome a colleague who is looking forward to work with us in a high-paced environment, while being faced with many deadlines.

About the department

Device Manufacturing Development (DMD), situated in Hillerød, is a project organisation with more than 600 engaged employees. We collaborate with Device R&D to create robust devices. We develop strong processes to ensure high quality, low cost and short lead time. We continuously improve products and production processes in collaboration with our stakeholders worldwide. 

The position is a part of the QC Development and Global Support team in Hillerød and is anchored in the Product Control and Global Support department. You will have 10 team colleagues, including Engineers and Specialists, who are dedicated to deliver test systems and documentation to our QC laboratories around the world.