Quality Engineer

Are you passionate about maintaining quality and handling deviations in a device manufacturing? Do you aspire to interact extensively with colleagues and stakeholders, while gaining a comprehensive understanding of the production lines?

If so, we are eager to welcome you as our new Quality Engineer in our dynamic team in Device Component Manufacturing (DCM). Read on and apply today!

The Position

As a Quality Engineer, you will be contributing to maintaining and developing quality and compliance of current production in DCM. This also entails playing a central role in ensuring the most effective, efficient, and compliant training and competence development best suited for the business area.

This role is central to quality management and reporting, covering a broad area within the business, with a wide range of stakeholders.

Your main focus will be on:
•    Managing quality documentation and conducting investigations in the production area to ensure compliance with our Quality Management System.
•    Contributing to the maintenance and enhancement of quality and compliance for current production within DCM.
•    Performing quality support tasks, including stakeholder meetings and KPI data updates.
•    Providing support to internal production, ensuring all parties involved adhere to GMP requirements.

Qualifications

To succeed in this role, you:
•    Hold a minimum of a bachelor’s degree in engineering, natural sciences, or a related field
•    Possess knowledge of Quality Assurance (QA) / Quality Control (QC) / International Organization for Standardization (ISO), Good Manufacturing Practice (cGMP) and quality-standards in a Lean set-up.
•    Showcase excellent organizational skills, proactively interacting with various departments, sites, and suppliers.
•    Display full professional proficiency in both spoken and written English, while having proficiency in Danish is a plus.

As a person, you are an excellent judge of character, inspiring motivator of others and can embrace continuous change. Being self-reliant but also act as an ambassador for cooperation, demonstrating adaptability, reliability, and a team-oriented mindset is crucial in this role. 

Being pragmatic and solution-oriented, while ensuring effective communication flow at all levels of organization and having great stakeholder management skills is key to succeed in our team. We will welcome a colleague who possesses strong analytical, planning, and prioritization skills, while excelling in a dynamic environment.

About the Department

Device Component Manufacturing (DCM) manages the production of high-quality components and preassembled parts for our internal customers within prefilled and durable devices. You will join DCM Production, which is responsible for ensuring high quality and effective manufacturing of moulded plastic components, and pre-assembled motor modules for prefilled pen systems in our internal production facility.

By joining us, you become part of a truly collaborative team, where colleagues are eager to exchange knowledge, as well as gain insights from your expertise. Within our team, we foster open communication, a positive mindset, and a strong enthusiasm for both personal and professional growth.

About Site Hillerød

Site Hillerød is an innovative and fast-growing production site. With over 4,000 talented employees, we work together to drive change for people living with serious chronic diseases. The site is located in beautiful natural surroundings, and we offer a diverse array of career paths at all educational levels. Join our vibrant community at Site Hillerød and ramp up your career while we ramp up our production! Get to know us better - visit our Site Hillerød career page Novo Nordisk Hillerød.

Working at Novo Nordisk

We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.

Contact 

For further information, please contact Manager Thue Elsen Nissen via email at tuen@novonordisk.com.

Deadline 

6 April 2025.

Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.

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.