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Test System Engineer in Devices & Supply Chain Management

Are you looking for a job where you play a key role in ensuring the quality of devices before they reach the hands of millions of people living with diabetes worldwide? Then we encourage you to keep reading as we are opening a new position as Equipment Engineer in our Device Laboratory in Device Manufacturing Development (DMD).

About the department
Device Manufacturing Development (DMD), situated in Hillerød, is a project organisation with more than 250 engaged employees. We collaborate with Device R&D to create robust devices. We develop simple & robust processes to ensure high quality, low cost and short lead time. We continuously improve products and processes in collaboration with our stakeholders worldwide.

The position is a part of the “Laboratory Support and Statistics” team in Hillerød and is anchored in the Pilot Operations team, that handles all operational activities of pilot and low volume devices related to purchase, planning, quality control and metrology, production as well as pack and delivery. You will have 13 new colleagues, including Technicians, Engineers and Specialists, who are dedicated to deliver test documentation that, ensure the authorities’ approvals of assembled devices.

The position
As Equipment Engineer in our Device Verification Laboratory, you will have various tasks and responsibilities. Firstly, you will be responsible for the maintenance of systems and equipment in the Device Laboratory. Additionally, you will act as Project Leader for the purchase of new equipment in compliance with standards and Novo Nordisk’s Quality Management System procedures and you will play a key role in the validation of new systems and equipment in the Device Laboratory. In particular, you will be part of the specification of equipment, test methods and data handling and you will be responsible for training of test personnel and regular process confirmation.

You will also handle change requests and non-conformities covering the full range of Novo Nordisk’s medical device and combination products. Another important part of the job is to ensure compliance in the Device Laboratory, so that we at all times live up to the requirements from the authorities, including preparation and implementation of necessary Standard Operating Procedures (SOP’s) and ensuring that we follow the SOP’s covering our functional area and train adequately.

The position gives you a great opportunity to develop your 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, Regulatory Affairs, other test departments in R&D, Quality Assurance (QA) and projects owners in pilot production and product maintenance.

Qualifications
Your background covers a Bachelor or Master’s degree in Engineering or similar. Ideally, you have gained experience with designing and executing test, with writing and review scientific documents with high technical complexity. You are familiar with GMP and Lean tools. Furthermore, it will be an advantage if you are familiar with handling and storage of electronic data and operating/maintaining of IT systems.

On a personal level, you demonstrate solid interpersonal and communication skills. Colleagues know you as a person with a proactive mind-set who enjoys building relations and collaborating across interdisciplinary boundaries. At the same time, you know how to support and motivate others to deliver on their targets. Additionally, you have a strong drive to deliver results in a high-paced environment with many deadlines. Lastly, you have written and spoken proficiency in both Danish and English.

Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

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

Deadline
1 March 2018.


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