Neurosoft Bioelectronics

Medical Equipment Manufacturing

1-10

Switzerland

At Neurosoft Bioelectronics we manufacture implantable medical devices meant to be used to treat neurological disorders.

The process engineer will:

*   Support all manufacturing activities (industrialization and validations) for medical devices, including supplier follow-up for components/ sub-assemblies delivery.
*   Participates in the incoming inspection of components, sub-assemblies and final devices.

**First round of applications will be open until May 25th 2023.**

## Tasks

**Manufacturing**

*   Performs processing of mechanical and electrical implantable medical devices in a controlled or cleanroom environment
*   Develops, configures and optimizes industrial processes
*   Provides support for all industrialization activities for implantable devices
*   Designs, runs, tests and upgrade systems and processes
*   Manages and follows the traceability files for all manufacturing activities
*   Provides support for manufacturing validation activities internally and externally
*   Provides support for tools and equipment calibration and maintenance

**Quality and documentation**

*   Writes and reviews manufacturing documentation and operating instructions and records, such as build instructions, work instructions and batch release forms
*   Describes the activities and/or the process in a simple, concise and legible way.
*   Reviews manufacturing-related documents to confirm that the information is correct, factual, exhaustive and with a good level of detail.
*   Provides support, to QA department, to perform incoming inspection

**Professional responsibility**

*   All activities are performed in accordance with Quality and Regulatory guidelines.
*   Maintain professional curiosity and knowledge of advancement and development in the field.
*   Willingness to acquire new knowledge specific to the field through continuing education.

## Requirements

**Education and experience:**

*   Bachelor's or Master's degree in engineering domain or equivalent
*   2-3 years of experience working in a cleanroom environment
*   Experience in working in an ISO 13485 environment with basic knowledge of EU requirements relative to the development and production of implantable medical devices
*   Fluent in English (written and spoken), French is an asset

**Specific skills**

*   Ability to prepare clear and concise documentation
*   Able to work with external manufacturers
*   Good communication
*   CAD or AutoCAD skills
*   Excellent technical skills
*   Will work in a cleanroom environment, as well as in a laboratory.

Our team is passionate about creating innovative solutions that can make a positive impact on people's lives. Working in a small team, you will have the opportunity to collaborate with experts in different fields, share your ideas, and contribute to the development of cutting-edge healthcare solutions. We value creativity, collaboration, and continuous learning, and provide opportunities for professional growth and development. If you want to be part of something truly special, we would love to hear from you.

Employee

Professional / Experienced

At Neurosoft Bioelectronics we manufacture implantable medical devices meant to be used to treat neurological disorders.
The process engineer will:
<ul>
<li>Support all manufacturing activities (industrialization and validations) for medical devices, including supplier follow-up for components/ sub-assemblies delivery.</li>
<li>Participates in the incoming inspection of components, sub-assemblies and final devices.</li>
</ul>
First round of applications will be open until May 25th 2023.
<h2 id="tasks">Tasks</h2>
Manufacturing
<ul>
<li>Performs processing of mechanical and electrical implantable medical devices in a controlled or cleanroom environment</li>
<li>Develops, configures and optimizes industrial processes</li>
<li>Provides support for all industrialization activities for implantable devices</li>
<li>Designs, runs, tests and upgrade systems and processes</li>
<li>Manages and follows the traceability files for all manufacturing activities</li>
<li>Provides support for manufacturing validation activities internally and externally</li>
<li>Provides support for tools and equipment calibration and maintenance</li>
</ul>
Quality and documentation
<ul>
<li>Writes and reviews manufacturing documentation and operating instructions and records, such as build instructions, work instructions and batch release forms</li>
<li>Describes the activities and/or the process in a simple, concise and legible way.</li>
<li>Reviews manufacturing-related documents to confirm that the information is correct, factual, exhaustive and with a good level of detail.</li>
<li>Provides support, to QA department, to perform incoming inspection</li>
</ul>
Professional responsibility
<ul>
<li>All activities are performed in accordance with Quality and Regulatory guidelines.</li>
<li>Maintain professional curiosity and knowledge of advancement and development in the field.</li>
<li>Willingness to acquire new knowledge specific to the field through continuing education.</li>
</ul>
<h2 id="requirements">Requirements</h2>
Education and experience:
<ul>
<li>Bachelor&#39;s or Master&#39;s degree in engineering domain or equivalent</li>
<li>2-3 years of experience working in a cleanroom environment</li>
<li>Experience in working in an ISO 13485 environment with basic knowledge of EU requirements relative to the development and production of implantable medical devices</li>
<li>Fluent in English (written and spoken), French is an asset</li>
</ul>
Specific skills
<ul>
<li>Ability to prepare clear and concise documentation</li>
<li>Able to work with external manufacturers</li>
<li>Good communication</li>
<li>CAD or AutoCAD skills</li>
<li>Excellent technical skills</li>
<li>Will work in a cleanroom environment, as well as in a laboratory.</li>
</ul>
Our team is passionate about creating innovative solutions that can make a positive impact on people&#39;s lives. Working in a small team, you will have the opportunity to collaborate with experts in different fields, share your ideas, and contribute to the development of cutting-edge healthcare solutions. We value creativity, collaboration, and continuous learning, and provide opportunities for professional growth and development. If you want to be part of something truly special, we would love to hear from you.

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