Technical Lead - Electronics Medical Device

Vertragsart:
Vor Ort
Start:
10/2018
Dauer:
01/2019
Von:
Michael Bailey Associates - Munich
Ort:
Basel
Eingestellt:
21.07.2018
Land:
flag_no Schweiz
Projekt-ID:
1602582

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We are recruiting for a technical lead who will undertake development project activities for electronic components of medical devices used in combination products such as auto-injectors and pumps.

Responsibilities:

  • Lead technical development activities for electronic components of medical devices used in combination products, eg auto-injectors, pumps
  • Specify requirements (DIR) of electronic components and define component strategy for future component platforms
  • Consider power management with an emphasis on ultra-low current and battery optimization for extended shelf-life of products
  • Collaborate with mechanical design engineers in the integration of electronic components in the product design
  • Collaborate with human factors engineers in the selecting appropriate electronic components for human interface including buttons, displays, speakers
  • Collaborate with Embedded software engineers to ensure hardware requirements are met
  • Work with third party suppliers for detailed design and development of electronic components and to ensure a robust process is followed (specifications, risk analysis, schematics and PCB layout, testing)
  • Planning, executing and reporting on design verification and robustness testing including storage, transport, in-use over defined life-time and misuse cases such as drop and water immersion
  • Work with third party suppliers to establish robust manufacturing process of electronic components and map critical to quality design requirements to manufacturing controls
  • Ensure components are delivered and controlled to the required quality for clinical trials and commercial production.
  • Report in to the Device Project Leader and Delivery System Leader on all technical aspects related to the device development project.
  • Generate Design Controls documentation while contributing to a high-quality Design History File (DHF) for parenteral delivery injection systems. Author and Reviewer of DHF documents such as Design Input Requirements, Component Specifications, Design Verification Plan and Verification Summary Report. Ensure quality and compliance to applicable regulations of the DHF elements of the assigned projects.
  • Ensure device design development in compliance with the regulations and delivered to a high quality.
  • Root cause analysis of out-of-specification product and develop robust solutions to prevent re-occurrence.

Requirements:

  • An ideal candidate would have at least 8 years of experience in electronics device development with main focus on medical devices for parenteral administration.
  • The ideal candidate would have experience generating DHF documentation, including but not limited to design input requirements, technical specifications, design verification, design validation, and design transfer. They are organized and structured in their approach and able to drive a technical team to reach solutions that meet with drug development milestones.
  • Excellent technical writing skills (eg, Design Controls)
  • Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)and of combination products (US) and standards, General understanding of Human Factors Engineering and Risk management
  • General understanding of pharmaceutical development

Michael Bailey International is acting as an Employment Business in relation to this vacancy.