Moulding Engineer

• Manufacturing
• Hillerød

Moulding engineer within Moulding Test Centre

Would you like to work as process responsible in a project organisation bringing innovative medical device concepts from development to launch readiness? Does your mindset include an unrelenting focus on quality in everything you do, and are you familiar with injection moulding? Then you may be the perfect match for our Moulding Test Centre.

The unit Device Manufacturing Department (DMD) is a project organisation comprising more than 250 engaged employees who all strive to achieve becoming the best manufacturing development partner of medical devices. Our dedication is to build superior quality into robust device products suitable for high volume production.

DMD Pilot Operations is a flexible development and test facility that supports device development from early R&D development stages into a stable production to market. In the Moulding Test Centre our focus is to perform explorative tests and optimize and validate injection moulding processes. We service our stakeholders by testing machines, moulds, mould concepts, materials etc. ensuring reproducibility and the optimum of technical, economic and environmentally sustainable solutions. You will be part of the Moulding team consisting of 12 engaged and dedicated colleagues, where you will be responsible for the moulds in our injection moulding test centre.

The position

As process responsible for moulding tools your primary responsibility will be to support verification and validation of moulding tools and components. You will work closely together with our skilled technicians performing the tests and our stakeholders requesting the tests. In a regulated GMP environment documentation of high quality is key but you should be able to balance the different requirements needed for explorative tests and production to clinical studies.

Together with the team’s equipment responsible you should also support tests, validation and documentation of other equipment related to the Moulding Test Centre and on a longer perspective act as substitute.

You will play an active role in an everchanging environment where assignments and priorities often change and in cooperation with colleagues inside and outside the department you will be responsible for adapting the quality and compliance level.

Qualifications

You hold a relevant degree within engineering with knowledge and understanding of the injection moulding process.

You have knowledge and experience within documentation of quality and compliance in relation to GMP and on a personal level, you are known for dedicating yourself to work proactively in order to solve the tasks at hand.

You face challenges with a positive and open mind-set in order to find the best solution in collaboration with our stakeholders. Furthermore, you can make independent decisions and navigate in a complex regulatory environment.

You are fluent in Danish and English (both written and oral) and have excellent communication skills as the job requires you to interact with many different stakeholders. Experience with TIMS3 is an advantage.

Contact
For further information, please contact Claus Munk Mikkelsen +45 3075 9590.

Deadline

The application deadline is 31 August 2020. Interviews will be held on an ongoing basis. Applications in Danish are also welcome.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.