Mechanical Engineer DDS

3 settimane fa


Milano, Italia Stevanato Group A tempo pieno

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 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.
  • The Sr. Mechanical Engineer interprets product development in a 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 coordinates engineering resources from external design agencies in a co-development environment.

Qualifications

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 of experience 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 a small group of engineers and or external consulting firms.
  • Fluent in oral and written English.

Preferred Qualifications:

  • Prior experience in Medical devices 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 to Stevanato Group’s Values: Trust and respect everyone; Be accountable; Be ethical, always; Listen and communicate with transparency and honesty; Deliver results.

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