Regulatory Affair Specialist Ii

hace 1 mes


Tijuana, México Emprego MX A tiempo completo

**Descripción y detalle de las actividades**
- Merit Medical México sigue creciendo y queremos que seas parte de nuestro desarrollo.

**Experiência y requisitos**
- Educación y/o experiência equivalente a una Licenciatura o Ingeniería. - Experiência: +4 años de experiência relacionada. Conocimiento de las reglamentaciones de la FDA de EE. UU., la Directiva de dispositivos médicos (93/42/EEC, modificada) y Normas del Sistema de Calidad ISO 13485. Automotivado, autodirigido, gran atención a los detalles y excelentes habilidades de gestión del tiempo. Sólidas habilidades interpersonales y la capacidad de comunicarse bien, verbalmente y por escrito, con los demás. Habilidades informáticas demostradas, preferiblemente hojas de cálculo, procesamiento de textos, base de datos, investigación y otros programas de software aplicables. Presentación reglamentaria/preparación de fundamentos. Asistencia con informes de vigilancia y dispositivos médicos. Habilidades informáticas/investigación en Internet. Habilidades de comunicación interpersonal. Asistencia con el desarrollo/capacitación del sistema regulatorio. Inglés conversacional.

**Organización**
- Merit Medical**Giro**
- Manufacturera**Actividad principal**
- Merit medical is a leading manufacturer of medical devices.**Número de empleados**
- 1300**Número de vacantes** 1**Área** Calidad**Contrato** Permanente**Turno** Diurno**Jornada** Tiempo Completo**Estudios** Titulo Profesional**Sexo** Indistinto



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