Robust and state-of-the-art automation processes are crucial to run an efficient and effective production, delivering high quality components to the assembly process resulting into a safe and reliable medical device for the patient.
Would you like to use your automation expertise and play a crucial role along the journey from concept development to full scale operation?
Do you want to develop state-of-the-art manufacturing solutions for medical devices?
If you want to join us on our growing journey and support the ramp up, or join our daily operations, then look no further! Apply today and be part of our Device Manufacturing & Sourcing II (DMS II) department.
Apply for Automation Engineer role now!
The position
As Automation Engineer you will be responsible for the automation equipment inside the plant. This includes equipment such as box exchangers, sorting chutes, and take-out robots (including end-of-arm tools) integrated with injection moulding workcells. But it also involves automation equipment around assembly lines. And intralogistics solutions, such as AGV’s and conveyer systems, to transport components and pre-assemblies, individual or in trays/boxes, between production processes and warehouse. 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, you could be the process owner who is responsible for ensuring flawless, safe, and compliant operation of the equipment.
As such, you will:
Participate in requirement definition and concept design of new equipment.
Participate in design reviews and acceptance testing, including review and approval of relevant documents.
Participate in the development of training plans and material for operators and technicians.
Develop operational procedures and instructions, and service and maintenance plans in close collaboration with equipment suppliers, technicians, and operators.
Contribute to validation approach. Write test and validation protocols and reports and support the execution of tests and validation activities.
Monitor operational performance of the equipment based on data and ensure that the validated state is maintained, troubleshoot issues. Initiate and drive improvement initiatives.
Oversee the procurement, manufacturing, factory acceptance testing and validation of new equipment as part of capacity expansions. Facilitate technology transfer to CMO’s and provide global support to Novo Nordisk owned equipment placed at CMO’s.
The job is located in Odense, but for the first 1-2 years frequent travel to the Hillerød/Greater Copenhagen area will be required. You should also expect international travel to equipment vendors and CMO’s.
