Process Responsible

Category:

Manufacturing

Would you like to be part of a project organisation dedicated to bridging innovative medical device concepts from development to launch readiness? Are you driven by a commitment to excellence in all aspects of your work and bring knowledge of injection moulding?

If this resonates with you, then you may be the perfect match for our Moulding Test Centre. Apply now and become part of our team, where you can contribute to shaping the future direction and refining our processes!

The position

As Process Responsible, your primary activity involves supporting verification and validation of moulding tools and components. You will work closely with our skilled technicians and stakeholders in performing the tests.

Some of your key tasks include:

• Preparing for and coordinating validation of moulding tools, acting as responsible for tool handling, and tool storage within the Moulding Test Center
• Coordinating and executing systematic problem-solving on production and processes issues
• Balancing effectively the different requirements needed for explorative tests and production to clinical studies in a regulated GMP environment
• Establishing and maintaining relevant data flows maps and data integrity risk assessments, driving process compliance
• Participating as an active member in the department, providing expert advice and guidance

Collaborating with the team’s equipment responsible, you should also assist in performing tests, validation activities, 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 in- and outside the department you will be responsible for adapting the quality and compliance level.

Qualifications

To be successful in this role, we believe you:

• Hold a relevant engineering degree, coupled with a strong grasp of the injection moulding process
• Possess expertise within documentation of quality and compliance according to GMP
• Demonstrate solid communication skills and adept stakeholder management
• Showcase proficiency in both spoken and written English

It would be considered as a strong advantage if you display fluency in Danish.

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 to find the best solution in collaboration with our stakeholders. Furthermore, you can make independent decisions and navigate in a complex regulatory environment, proactively interacting with various colleagues and teams.

About the department

DMD is a project organisation comprising more than 600 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 10 engaged and dedicated colleagues, where you are responsible for the moulds in our injection moulding test centre. As part of a truly international team, you can look forward to being met by colleagues who 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.

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 Claus Munk Mikkelsen at +45 3075 9590.

Deadline

9 June 2024.

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 to 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.