Systems Engineer - Medical Devices

Basel  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Description

We are looking for a Systems Engineer for a Global Medical Device company focusing on the development of new state of the art Combination/drug delivery devices. The System Engineer will contribute to the development of best-in-class system engineering practices and its implementation to medical device and/or software as medical device (SaMD) development projects. You will have practical experience covering the product development to the life cycle management. As an expert, you will work with cross-functional teams and support various development activities including system conceptualization, system requirements, risk assessment, system verification and validation.
Responsibilities:
  • Design and implement systems engineering approach to support the development and life cycle management of complex products and platforms in the areas of drug delivery devices, digital technologies, and SaMD.
  • Utilize the systems engineering tool for requirement management and translate user and business needs into systems/sub-system requirements
  • Actively maintain and monitor the traceability from the requirements to the verification activities
  • Be the representative of systems engineering for the communications with cross-divisional teams, programs, and stakeholders
  • Author relevant design history files and GMP compliant documentations
  • Work within development projects with cross-functional teams, provide the system-level views and guide the projects to use the structured approach for product development


Academic Requirements:
  • Bachelor or more advanced degrees in Biomedical Engineering, Systems Engineering, Electrical Engineering, Computer Science, or other relevant disciplines


Professional Requirements:
  • Prior experience with design control processes, product lifecycle management in a GMP environment
  • Expert knowledge in Systems Engineering and Risk Management
  • Experience working with detailed requirements and traceability in order to author requirement documentations
  • Knowledge in system functional modeling and/or programming ability using system modeling language (SysML) is highly preferred.
  • Well-versed in medical product development, Quality Management System, and regulatory processes (ISO 13485, 60601, 62304)


Kontakt: Luchele Mendes

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start date
01/2019
Duration
01/12/2019
From
Michael Bailey Associates
Published at
13.12.2018
Project ID:
1688290
Contract type
Freelance
To apply to this project you must log in.
Register