Are you a seasoned injection moulding expert looking to apply your technical subject matter knowledge to develop state-of-the-art manufacturing solutions for medical devices? Would you love to be part of Novo Nordisk’s growing journey and support the ramp up to full scale production – or even join daily operations? Then look no further! Take this rare opportunity and join our Device Manufacturing & Sourcing II (DMS II) department.
The position
We are looking to recruit 2 different positions:
Tooling Engineer : As Tooling Engineer you will be responsible for the injection moulding tools used to produce plastic device components in our plant and at our Contract Manufacturing Organisations (CMOs). You play a crucial role along the journey from concept development to full scale operation. You collaborate closely with project managers and colleagues in device manufacturing development, bringing in valuable insights and requirements from an operational point of view. Upon finalization of the development and validation phase, you could be the process owner who is responsible for ensuring flawless, safe, and compliant operation of the different tools running around the world.
Moulding Machine & Auxiliary Equipment Engineer : As Moulding Machine & Auxiliary Equipment Engineer you will be responsible for the injection moulding machines used to produce plastic device components in our plant, including auxiliary equipment such as dosing unit, mixer/blender, thermolator, heats & servo controller, etc. You will play a crucial role along the journey from concept development to full scale operation. You will collaborate closely with project managers and colleagues in device manufacturing development, bringing in valuable insights and requirements from an operational point of view. Upon finalization of the development and validation phase, you could be the process owner who is responsible for ensuring flawless, safe, and compliant operation of the equipment.
Both positions are located in Odense, but for the first 1-2 years, frequent travels to Hillerød/Greater Copenhagen area will be required. You should also expect international travels to equipment vendors and CMO's.
In both positions, you will:
Participate in requirement definition, concept design of new equipment, design reviews and acceptance testing, including review and approval of relevant documents
Take part in the development of training plans and material for operators and technicians
Develop operational procedures and instructions, as well as service and maintenance plans in close collaboration with equipment suppliers, technicians, and operators
Contribute to validation approach: writing test and validation protocols and reports as well as supporting the execution of tests and validation activities. You will also oversee the procurement, manufacturing, factory acceptance testing and validation of new equipment as part of capacity expansions
Monitor operational performance of the equipment based on data and ensure that the validated state is maintained, troubleshoot issues
Initiate and drive improvement initiatives as well as facilitating technology transfer to Contract Manufacturing Organisations
Qualifications
To be considered for those positions, we imagine you:
Hold at least a Bachelor’s degree in Engineering or any other related field
Have a previous work experience with injection moulding, ideally obtained within a manufacturing development and/or GMP production of medical devices, including process validation
Be fluent in English, both written and spoken