Este puesto ya no está disponible.

Instrument Development Engineer (H/F) - CDI

Indefinido
Villejuif
Salario: No especificado
Sin trabajo a distancia

Stilla Technologies
Stilla Technologies

¿Te interesa esta oferta?

jobs.faq.title

El puesto

Descripción del puesto

Stilla is hiring an Instrument Development Engineer, whose main mission will be to develop hardware modules of Stilla’s new instruments.

Our ideal candidate:
• Has one or more successful experiences taking part in the hardware development of an In-Vitro Diagnostic instrument
• Has an Engineering degree in Mechanics, Electronics or Embedded Software.
• Has a good knowledge of quality & regulatory standards in the field, ex. ISO 13485,
IVDD/ IVDR, EN61010-1, MDSAP.
• Has a proven track record in coordinating external partners
• Likes to interact with multi-disciplinary teams
• Must speak French and English fluently

Missions for the Instrument Development Engineer

The Instrument Development Engineer leads the development of one or several STILLA instruments modules, including hardware and firmware.
He/she is responsible for developing the module(s) in accordance with instrument specifications, as well as quality, timeline, and budget constraints of the development.

  1. Manage the development of instrument modules
    • Plan in detail the module development, track progresses and ensures quality, delays and development costs constraints are respected
    • Coordinate and follow-up a team of technician and engineer (software, mechanics, …)

  2. Develop the instrument module(s)
    • Participate in instrument functional analysis and architecture
    • Participate in instrument and module risk & failure mode analysis
    • Perform or outsource feasibility studies
    • Write module(s) technical specifications
    • Design or outsource module(s) components: mechanical parts, PCB, firmware
    • Monitor the outsourced development and report the progress
    • Build and setup modules prototypes
    • Test or oversee the test of the prototypes
    • Participate to the integration of the module(s) in the instrument
    • Create and maintain documentation compliant to ISO 13485

  3. Transfer to Production and Product Life Management
    • Transfer technical knowledge to the Operations team
    • Support Operations team in solving non-conformities and participate in CAPA teams
    • Ensure continuous product improvement based on customer feedback, and document change management on the instruments


Requisitos

Why join us?
• Join a young and dynamic Life Science company growing at a 3-digit pace!
• Work with a team who shares a passion for building successful Life Science Products based on deep technological innovations.

Location:
Main office: Roanne (Loire)
Frequent travels to Stilla Villejuif, Occasional travels in France and worldwide

¿Quieres saber más?