Quality Supporter

Are you THE facilitator of problem solving on a professional level, and THE driver of the handling of deviations, from initial discovery to the implementation of corrective and preventive measures on the production lines? Are compliance and efficiency core values for you as an individual? Do you have a systematic yet creative mindset to pursue robust solutions that create value for your customers?

Then this is your call for action! Device Manufacturing & Sourcing is looking to expand our team with quality engineers that use systematic problem-solving techniques to solve our biggest quality related projects.

The Position

The main purpose is to safeguard patient safety and improve product quality by ensuring a high-quality root cause investigation and the right corrective actions. Your job area will be within medical devices and covers several different technologies within advanced injection moulding, metal components and assembly.

you are expected to play a key role on:

• To handle deviations related to medical devices from our production.
• Driving / facilitating root cause investigations together with process experts, Quality Assurance and Production.
• Pursuing robust countermeasures with positive impact in product quality, patient safety, compliance and process efficiency.

You should thrive in building relations and expanding your knowledge in a complex and challenging business environment. You will find that you have rich opportunities to create great results and develop yourself, both on a professional and on a personal level, and you will be trusted to execute your great ideas.

Qualifications

To be successful in this role, you will need to have the following requirements:

• You have an academic degree with a technical background within engineering and/or natural/pharmaceutical sciences.
• You either speak Danish or you have an interest in learning the language.
• You have a previous experience with systematic problem solving, root cause analysis and deviation obtained within quality assurance, moulding or assembly.
• You are used to working in compliance with quality and GMP requirements and you demonstrate a LEAN mindset.
• Knowledge and experience with working in a highly regulated GMP environment is an advantage.

It is an advantage if you have:

• Experience with working in a production environment.
• Mechanical understanding of CAM and/or servo-controlled machines, is an advantage, but not a requirement.
• Experience with project management.
• Handling of costumer complaints.

If you do not meet all the requirements above but you share our passion for quality, regulations and problem-solving and are keen to acquire professional competencies we want to hear from you.

As a person, you possess excellent communication skills and excel in establishing relations with other people. You bring a positive mindset, are straightforward, and have a systematic approach to problem-solving. You are proactive and have a great interest in developing yourself and the team you are a part of. Finally, you are curious and seek to understand the underlying complexities and gain energy by going on the shop floor and interacting with your stakeholders and your team.

About the Department

You will join Pre-assembly Production in Hillerød, Denmark. We are approximately 200 colleagues, working in 10 teams, and we produce the mechanical Motor Module in Novo Nordisk’s newest prefilled devices FlexTouch® and FlexPro®. We deliver large quantities to our sister factories in Diabetes Finished Products and Biopharmaceuticals. The department also function as centre of excellence that handles improvements, upgrades and expansion of production capacity with a global production perspective. You will work closely with 10 experienced and dedicated colleagues in Pre-Assembly Quality, Training and Improvement team, whom the main purpose is to safeguard patient safety and improve product quality by ensuring a high-quality root cause investigation and the right corrective actions.

Working at Novo Nordisk

Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.

Contact

Please contact Associate Manager, Thue Elsen Nissen (+45) 34481980 for further information.

Deadline

May 8, 2024

Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.

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.