Injection Moulding Coordinator
Hillerød, Capital Region of Denmark, DK
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 an Injection Moulding Coordinator, you will serve as the primary point of contact for stakeholders seeking support with test runs in our Moulding Test Centre. You will be responsible for identifying the best fit between mould and machine, coordination of test plans, and ensuring smooth execution.In the longer term, you will also take part in preparing validation protocols for the introduction of new device components.
Some of your key tasks include:
- Planning of test runs and production in our injection moulding facility.
- Write test protocols for tests to be conducted in our test centre with input from our stakeholders.
- Support validation activities when new components or devices are to be introduced.
- Working closely together with our process responsibles and skilled technicians performing tests and our stakeholders requesting the tests.
- Balancing effectively the different requirements needed for explorative tests and production to clinical studies in a regulated GMP environment.
You will play an active role in a dynamic and fast-paced environment, where assignments and priorities often change. Working closely with colleagues both within and outside the department, you will be responsible for ensuring alignment and adherence to the plans, while maintaining flexibility to adapt as needed
Qualifications
To be successful in this role, we believe you:
- Hold a Bachelor’s degree within engineering, any other relevant field, in manufacturing, or similar.
- Have some experience with 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 and Danish.
On a personal level, you are known for dedicating yourself to work proactively 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
The unit Finished Product Manufacturing Science & Technology (FPMSAT) is a project organisation comprising more than 800 engaged employees who all contribute to become the best manufacturing development partner of medical devices. Our dedication is to build superior quality into robust device products suitable for high volume production.
Pilot Operations is a flexible development and test facility within FPMSAT that supports device development from early R&D development stages into a stable production to market. You will be part of the Moulding and Quality support team consisting of 10 engaged and dedicated colleagues whose main tasks are test runs on injection moulding tools and quality support across Pilot Operations.
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.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Claus Munk Mikkelsen cmum@novonordisk.com.
Deadline
10 June, 2025. We review applications and conduct interviews on an ongoing basis, so we encourage you to submit your application at your earliest convenience.
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.