Descripción y detalle de las actividades 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\-comforting 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. Experiencia y requisitos * 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 Beneficios * Beneficios de acuerdo a la LFT * fondo de ahorro **Número de vacantes** 1 **Área** Calidad **Contrato** Permanente **Modalidad** Presencial **Turno** Mixto **Jornada** Tiempo Completo **Horario*** Tiempo completo * Lunes a viernes **Estudios** Carrera con título profesional **Inglés** Hablado: Avanzado, Escrito: Avanzado **Disponibilidad p. viajar** No