Description and detail of the activities The Quality Supervisor in Production will be directly responsible for people and processes of a designated operations process area. This candidate will develop and improve processes using lean manufacturing techniques. This leader will provide team building, goal setting, and change management. Key Tasks \& Responsibilities: * Coordinates and supports regular inspection activities based on priority production and availability/training of Quality inspectors. Coordinates inspections and special tests for the release of products in validation or non\-conforming. * Inform QC manager about personnel, process, material and compliance concerns. * Notifies and coordinates inventory inspections of non\-conforming components that impact compliance with product specifications. * Investigate corrective action requests and identify / implement solutions. * Reviews and coordinates with leaders / inspectors the correct compliance to fill the quality records required in the inspection process to the products / processes. * Assure that product and process quality is compliant to internal, industry and customer quality standards. Experience and requirements * Bachelor Degree in Engineering * 2\+ years of relevant experience in medical device environment * Proficient verbal and written communication skills * Excellent interpersonal skills * English 80% * Proficient in Microsoft Word, Excel, and Outlook * Product and procedure training * ISO \& Quality overview Benefits * Benefits according to LFT * savings fund **Number of vacancies** 1 **Area** Quality **Contract** Permanent **Modality** In-person **Shift** Mixed **Workload** Full Time **Schedule*** Full time * Monday to Friday **Education** Professional degree **English** Spoken: Advanced, Written: Advanced **Travel availability** No