Production Technician

• Perform processing of mechanical and electrical implantable medical devices in acleanroom environment

• Set up and maintain workstation, while adhering to Controlled Environment requirements

• Perform production tasks, including equipment setup, operation, maintenance and calibration in line with QMS protocols.

• Manage traceability and documentation records for all manufacturing, calibration and maintenance activities.

• Support industrialization and validation activities for implantable devices, both internally and externally (such as external partners and suppliers).

• Collaborate with team for process and documentation improvements and provide technical support to projects.

• Monitor processes, conduct root cause analysis, and coordinate with stakeholders to minimize downtime.

• Maintain thorough documentation in accordance with ISO 13485 standards and comply with cleanroom and safety regulations.

• Provide feedback to the team regarding process and product improvements and actively participate to the continuous improvement of manufacturing practices.

• Strong technical and manual skills with attention to detail and accuracy.

• High level of manual dexterity for handling delicate components and performing intricate tasks.

• Excellent attention to detail, organization and precision in work, vital for maintaining product quality and integrity.

• Proficiency in documenting work reliably and accurately in compliance with QMS standards.

• Ability to work effectively in a team, contributing to a collaborative and supportive work environment, while also capable of working autonomously, independently handling routine tasks.

• Strong communication abilities to clearly share ideas, receive feedback, and report to supervisors.

• Strong commitment to health and safety regulations, demonstrating responsibility and accountability.

• Self-direction, with the ability to manage time effectively and take initiative in problemsolving.

• Adaptability and commitment to continuous learning, keeping pace with the rapid evolution of neurotechnology due to technological and regulatory changes.

• Practical experience and knowledge of Good Manufacturing Practices (GMP), ISO 13485 or other relevant regulatory requirements.

• Minimum 5 years of experience working in a cleanroom environment, ideally in medical device manufacturing.

• Ability to work under microscopes, with tweezers, micrometers, scales, and with other handheld tools for small parts.

• Mandatory good writing, reading and oral skills in English (B2) (i.e., read, understand manufacturing procedures and document records in English)

• Asset: initial training such as CFC or similar (BTS / DUT), or higher qualification.

Neurosoft Bioelectronics