Description

Your mission :

You actively participate in performance testing for Quality Controls (QC), Design Verification activities, equipment management, and stock management activities.

Key responsibilities and accountabilities :

Incoming inspection:

• Execute test protocols in laboratory environment. 
• Report test results and nonconformities in a timely manner. Stock management and delivery. 
• Support the follow-up and documentation of stock moves (e.g., inventory check).
• Support the preparation of delivery orders. Laboratory equipment management.
• Track the qualification status of the equipment and ensure their conformity in time. 
• Execute the equipment qualification protocol, including, as applicable, sending the equipment to supplier.
• Maintain the corresponding documentation. Contribute to establishing work instructions/protocols, and support process improvement.

System test : 

• Execute verification test protocols as part of Design Verification. 
  
• Execute characterization protocols as part of the Design and Development.

Specific responsibilities :

QC related tasks may be assigned (e.g., contribute to investigations in the frame root cause analysis, interacting with Supplier and logistic partners).

Knowledge, skills and abilities  :

• Technical know-how for executing protocols, performing simple measurements such as weights and pressures.
• Familiar with quality control and quality assurance. 
• Strong organizational skills and attention to detail.
• Good written written and oral communication skills.
• Knowledge of laboratory environment standard behaviors and requirements.
• Attention to detail and accuracy in conducting tests. 
• Collaborate with cross-functional teams to address and resolve quality-related issues, contributing to effective root cause analysis and corrective actions.
• Fluent in English, and preferably also in French.

Education and experience  :

• Technical experience in laboratory environment with relevant educational background.
• Experience with contributing to and executing work instructions/protocols.
• Experience in the field of quality in medical or another regulated industry in compliance with regulations (e.g., ISO, ISO 9001).
• Experience in the field of quality control, ideally in medical technology is a plus.

Start of the mission : as soon as possible

Activity rate : %

We offer :

• Participation to innovative projects being part of a team of experts.
• Access to latest technologies.
• A dynamic working environment where collaboration is one of the key elements

To apply : Please send your cover letter to along with your resumé.

Important remarks

For this particular position, please note that only candidates possessing a Swiss passport or those from UE-27/AELE living in Switzerland and having a permit B will be considered for reasons of long waiting in obtaining work permits for the other candidates.