Contribute to the development of new products and the improvement of current medical devices. This is achieved by working on both the hardware and software aspects of medical devices, documenting, and ensuring the products comply with various product-specific and regulatory standards and directives.
The role requires the ability to work on projects in different phases of development alongside various internal teams. Effective communication with scientific advisors and SMExe2x80x99s and external manufacturers or suppliers of goods and services is also essential.
Minimum Requirements:
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