Senior Mechanical Engineer DDS

Job Description

We are looking for a Sr. Mechanical Engineer to be inserted in our team of Design Center for Drug Delivery Systems in Milan (IT).

Role Introduction

• Will be part a of the Drug delivery system (DDS) Team an experienced and growing team of medical devices engineers that leads the development of proprietary devices for Stevanato Group.
• Work in a fast-paced, international and multi-disciplinary team within an entrepreneurial environment where it is possible to transform good ideas into real products.
• Will be involved in the mechanical development of drug delivery devices device.
• The Sr. Mechanical Engineer interprets product development in an holistic way, taking care of early concept development, CAD models, material selection, tolerance analysis, interaction for key suppliers, defining test methods and following industrialization activities.

Responsibilities

• Is responsible for the system or sub-systems mechanical development of drug delivery devices.
• Participate in all development activities from early stage concept definition to design reviews, from fast prototyping activity to design transfer to manufacturing.
• Works along and coordinate engineering resources from external design agencies in a co-development environment.

Minimum Qualifications

• 5-10 years of experience in end-to-end product development - from early design stage to mass production in heavily regulated markets (Medical / Automotive / Aerospace).
• 5+ years ofexperience with plastic component and mechanism design.
• Solid fundamentals in mechanical design (design for manufacturing, material selection, design for assembly, tolerance analysis).
• Hands on experience with mechanical modeling and simulation (structural and kinematic analysis, FEA).
• Master CREO / Solidworks or equivalent CAD system.
• Experience with New Product Introduction processes.
• Experience with common Risk Analysis techniques (FMEA, Fault Tree Analysis, etc).
• Prior experience coordinating small group of engineers and or external consulting firms.
• Fluent in oral and written English

Preferred Qualifications

• Prior experience in Medical device and drug delivery devices
• Knowledge of regulatory and standard guidelines such as : ISO 13485, ISO 11608, ISO 10993, ISO 14971, FDA / EMEA guidance documents.

Adherence toStevanato Group’s Values : Trust and respect everyone; Be accountable; Be ethical, always; Listen and communicate with transparency and honesty; Deliver results