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.  

Working at Novo Nordisk

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
 
Contact

For further information, please contact Senior Manager Lars Aagaard at +45 3079 2095.

Deadline

14 July 2024.

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 
 
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.