Stilla Technologies

Stilla Technologies

Instrument Verification Engineer

  • CDI 
  • Roanne
  • > 5 ans

Le poste

Instrument Verification Engineer

  • CDI 
  • Roanne
  • > 5 ans


Stilla Technologies is a Life sciences company whose mission is to improve health by offering researchers and clinicians worldwide solutions for high precision genetic analysis.

Since 2016, Stilla Technologies has empowered researchers with the naica® system, a solution that enables to detect & quantify nucleic acid with unprecedented precision.

The naica® system supports a wide range of genetic tests and molecular biology assays — including liquid biopsy tests for cancer diagnostics, viral load quantification, GMO detection, etc… Overall, the naica® system superior performances make it a preferred technology for precision medicine research and therapeutic monitoring.

Stilla® advises and supports its customers worldwide with a multidisciplinary team, whose expertise spans from microfluidics and chemistry to molecular biology and computer science. Stilla’s talented and multidisciplinary team shares a passion for building successful Life Science and Diagnostic products based on deep technological innovations.

Job description

Missions for the Instrument Verification Engineer

The Instrument Verification Engineer leads hardware and functional verification of one or several STILLA instruments.
He/she is responsible for building verification plans to cover instrument specifications. He/she is also responsible for the execution of the plans, performing the test himself/herself, and/or by driving internal and external resources.

  1. Manage the verifications
    • Plan and manage hardware and functional verifications activities on instruments development and sustaining projects, while ensuring delays and verification costs constraints are respected
    • Identify and manage material and team needs for the execution of the tests and verifications.
    • Manage on-site and off-site subcontractors taking part in the tests and verifications activities.

  2. Verify instruments specifications
    • Participate in instrument functional analysis, specifications definitions and risk analysis.
    • Define and document test and verification plans.
    • Participate in the settings of the instrument.
    • Execute test and verification plans, documenting results.
    • Perform physical measures on instruments hardware components.
    • Interface with Stilla Quality & Regulatory department on the instrument verifications versus specifications coverage documentation.

Preferred experience

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

Recruitment process

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.

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

Meet the team

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