Role: Senior Manager

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 skills and management experience to meet the challenges of developing combination products in a multi-project, multi-disciplinary setting.
• Lead and manage the creation and iteration of product designs from concept and through the preparation of detailed specifications and transfer to high volume manufacture.
• Applying solid engineering principles and your experience of device design, materials, manufacturing processes, finishing and assembly you will navigate complex constraints in the design space to achieve robust, cost-effective, functional device designs and coach others to do the same.

• First or upper second mechanical engineering degree.
• Excellent people management skills and experience
• Strong technical skills and passion for mechanical engineering and mechanism design.
• Tangible experience of design for manufacture of high-volume moulded parts and assemblies for medical or drug delivery applications
• Experienced with 3D CAD; Creo and/or Solidworks, analysis of tolerances, and simulation techniques (FEA, CFD) as applied to development of high-volume products
• Awareness of the principles of Design Control within ISO 13485 & FDA 21 CFR Part 820.