Role: Principal Engineer, Device Design Industrialisation

Location: Northern Cross, Dublin

Benefits: Excellent salary, Annual bonus: 8%, Annual salary reviews, VHI Healthcare from Day 1 Covers the employee, their spouse and children up to the age of 18, Includes the Employee Assistance Programme (Counselling, specialist information and coaching service, Life insurance, Private pension, 23 days of annual leave, Sick leave, Subsidised canteen, Bike to work scheme, Tax saver for public transport, Sports & social club, Cark parking, Reimbursement for additional trainings and courses


Company:
My client is a Global Healthcare organisation is focused on the design, development and commercialisation of a diverse portfolio of device technology solutions to enable delivery for our large and growing range of generic and branded products around the globe.


Key responsibilities for this role include:

• Working within design teams to develop drug delivery devices, you will apply your technical knowledge and experience of tooling, moulding, metrology and problem-solving ability to meet the challenges of industrialisation of new medical devices for respiratory and injectable drug delivery.
• Applying your knowledge of materials, processing, process capability and statistics, mould flow simulation, tool qualification, metrology, high-volume component manufacturing processes and complex assembly processes to enable the development of cost-effective and robust components and assemblies.
• Negotiating competing design and manufacturing requirements within our multi-disciplinary teams to de-risk the development process and deliver practical solutions for robust device designs that achieve performance, reliability and manufacturing requirements, capable of scale up to high volumes.

• Mechanical engineering degree or engineering apprenticeship with substantial experience of tooling, moulding, and cGMP manufacture
• Experience in the design for manufacture and industrialisation of medical devices and combination products
• Awareness of the principles of Design Control within ISO 13485 & FDA 21 CFR Part 820.
• International travel will be required as part of this role.