• Manufacturing
• Hillerød

Are you looking for the opportunity to make our patients’ lives better and leave your footprint! Then maybe you are the "Technical Project Engineer" we need for exciting projects the next two years.

About the department:
Moulding Equipment Support (MES) – Projects is an important part to continuously improve our processes ensuring timely delivery of our products without compromising on quality. MES is a part of Moulding and Quality Support that supports all stakeholders across externally production suppliers of plastic components. Our main tasks are to drive projects to support all our stakeholders in ramping up production capacity, improving the existing fleet of equipment and above all to ensure that the supply of high-quality components is never compromised.

The team is located in Hillerød and consist of highly experienced technical project engineers that are individually chosen for their expertise and experience from several years in production and quality areas. They strive to support each other, simplify by always being curious and empower by trusting each other in every task.

We offer you an exciting position where you will contribute with your relevant experience and where you are guaranteed to learn and develop your skills within decoration/printing and handling of plastic components as well as your project management skills. You will have a wide contact interface within the department and be empowered to provide the best support to all your stakeholders. You will also be part of a team that is high performing every day and have fun at the same time!

The position:
As a Technical Project Engineer your key responsibility will be to support and drive projects in the project team in the Moulding and Quality support department. Key deliverables are mainly focused on driving and managing projects related to GMP compliance and validation.

Key success criteria will be to drive and support projects for validation of machinery or equipment such as decoration/printing equipment or handling units. Furthermore, you will be involved in implementation and preparation of documents and execute the necessary projects to present during inspection and audits. You will be responsible for conducting validation plans and documents related to specification, risk assessment, FAT, SAT, IQOQ and PQ activities etc. In everything you do, you will be responsible for GMP compliance and readiness for inspection within scope of projects as well as drive or initiate continuous improvements or projects, to increase safety, quality, compliance, output, and stability.

Hence, you need to have a strong technical understanding, being able to generate new ideas and provide thorough quality, compliance and development of processes. You will support projects running at global sites in Denmark, USA, Ireland, Czech Republic and Brazil.

The postion is a 2-year temporary position.

Qualifications

You hold min. a BSc. within relevant field of engineering + 2 years of experience. Furthermore, you have experience within Good Manufacturing Practice (GMP), knowledge of automation and/or printing or decoration processes and experience with project execution.

As a person you are ambitious, proactive and have the ability to interact with people at all levels in the organisation. You have technical understanding, a good quality mind-set, and solve problems independently as well as through cooperation when applicable. You execute tasks in a timely matter and with continuous communication towards stakeholders.

Furthermore, you write and speak English and are able to communicate technical complex issues easily.

Working at Novo Nordisk
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes, obesity and other therapy areas. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.

Contact

If you want to hear more about the position, please contact: Signe Steninge Jacobsen on +45 3079 9700

Deadline

10 May 2020. Interviews will be conducted on an ongoing basis.

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.