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Participa en la resolución de cualquier responsabilidad legal y en el cumplimiento de las normativas gubernamentales. Garantiza una recepción, mantenimiento y evaluación precisos respecto al etiquetado del producto. Informa sobre eventos o reacciones según lo requieran las agencias reguladoras, incluyendo datos de eventos adversos procedentes de estudios clínicos, fuentes espontáneas o solicitadas, informes periódicos y de experiencia. Puede proporcionar detección y evaluación de señales de tendencia y seguridad. Apoya todas las actividades de experimentación clínica y postcomercialización.\n### **Acerca del puesto**\n\nPrincipales responsabilidades \n\n \n\n\\~ Apoyar la gestión de los procesos operativos para garantizar el cumplimiento de los procedimientos globales/locales de Novartis, así como de las normativas/normas/guías nacionales e internacionales sobre farmacovigilancia de productos comerciales e investigacionales de Novartis\n \n\n\\~ Gestionar la recopilación, el procesamiento, la documentación, la notificación y el seguimiento de todos los informes de eventos adversos (AE) para todos los productos Novartis provenientes de estudios clínicos, estudios postcomercialización (PMS), programas orientados al paciente (POP), registros y todos los informes espontáneos (SR).\n \n\n\\~ Transcribir, traducir (cuando sea necesario) e introducir con precisión y coherencia los datos de todos los eventos adversos graves (de estudios clínicos) y de todos los eventos adversos (de POP, PMS, registros y todos los SR) desde los documentos originales a los sistemas de seguridad, haciendo hincapié en la puntualidad y calidad.\n \n\n\\~ Registrar y hacer seguimiento de la recepción, envío y distribución de documentos como SAE, SR, notificaciones de investigadores, etc., en colaboración con otros departamentos\n \n\n\\~ Gestionar la notificación/envío/distribución de informes/actualizaciones/información de seguridad a las Autoridades Sanitarias Locales y/o a las operaciones clínicas, en colaboración con otros departamentos.\n \n\n\\~ Colaborar con otros asociados de fotovoltaica locales/globales para garantizar una evaluación precisa de los datos de seguridad.\n \n\n\\~ Interactuar e intercambiar información de seguridad relevante con LHA, asociados de fotovoltaica, otros grupos funcionales y contratistas de terceros, si corresponde.\n \n\n\\~ Detectar y monitorear las normativas globales/regional/nacionales (casuales) sobre farmacovigilancia y proporcionar actualizaciones a la organización global de PVO.\n \n\n\\~ Desarrollar, actualizar e implementar procedimientos locales para garantizar el cumplimiento de los procedimientos globales de PVO y los requisitos nacionales.\n \n\n\\~ Gestión y mantenimiento de todas las bases de datos PVO asignadas pertinentes, si corresponde.\n \n\n\\~ Desarrollar y actualizar materiales de formación para farmacovigilancia\n \n\n\\~ Garantizar el apoyo y cierre de auditorías, actividades del plan de acción correctiva y visitas de inspección de la autoridad sanitaria.\n \n\n\\~ Proporcionar información oportuna y pertinente a coordinadores de ensayos, AGENCIAS y otro personal de Novartis\n \n\n\\~ Distribución de muestras promocionales (si corresponde) \n\n \n\nIndicadores clave de rendimiento \n\n \n\nSupervisa y controla el programa de vigilancia de medicamentos, biológicos o dispositivos médicos de la empresa, incluyendo la recepción, evaluación, procesamiento y seguimiento de los informes de reacciones adversas. Participa en la resolución de cualquier responsabilidad legal y en el cumplimiento de las normativas gubernamentales. Garantiza una recepción, mantenimiento y evaluación precisos respecto al etiquetado del producto. Informa sobre eventos o reacciones según lo requieran las agencias reguladoras, incluyendo datos de eventos adversos procedentes de estudios clínicos, fuentes espontáneas o solicitadas, informes periódicos y de experiencia. Puede proporcionar detección y evaluación de señales de tendencia y seguridad. Apoya todas las actividades de experimentación clínica y postcomercialización. \n\n \n\nExperiencia laboral \n\n \n\n\\~ Gestión y ejecución de operaciones \n\n\\~ Colaboración interempresarial \n\n\\~ Extensión funcional \n\n \n\nHabilidades \n\n \n\n\\~ Archivado (documentos) \n\n\\~ Farmacovigilancia \n\n\\~ Ciencia de la seguridad \n\n\\~ Bases de datos \n\n\\~ Formación de empleados \n\n\\~ Crónica \n\n \n\nIdioma \n\n \n\nInglés\n**Por qué Novartis:** Ayudar a las personas que padecen enfermedades y a sus familias requiere más que ciencia innovadora. Requiere una comunidad de personas inteligentes y apasionadas como tú. Colaborando, apoyándose e inspirándose mutuamente. Unidos para lograr avances que transformen la vida de los pacientes. ¿Listo para crear un futuro mejor juntos? https://www.novartis.com/about/strategy/people\\-and\\-culture\n\n**Únete a nuestra red de Novartis:** ¿No es este el puesto adecuado en Novartis para ti? Regístrate en nuestra comunidad de talentos para mantenerte conectado y conocer oportunidades profesionales adecuadas tan pronto como surjan: https://talentnetwork.novartis.com/network\n\n**Beneficios y recompensas:** Consulta nuestro manual para conocer todas las formas en que te ayudaremos a prosperar personal y profesionalmente: https://www.novartis.com/careers/benefits\\-rewards\n\n\n \nDivisión\nDesarrollo\nUnidad de negocio\nMedicamentos Innovadores\nUbicación\nArgentina\nSitio\nRamallo (Argentina)\nEmpresa / Entidad Legal\nAR01 (FCRS \\= AR001\\) Novartis Argentina S.A.\nÁrea Funcional\nInvestigación \\& Desarrollo\nTipo de trabajo\nTiempo parcial\nTipo de empleo\nRegular\nTrabajo por turnos\nNo","price":"Salario negociable","unit":"per year","currency":null,"company":"Indeed","language":"es","online":1,"infoType":1,"biz":"jobs","postDate":"1761112248000","seoName":"patient-safety-specialist","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://ar.ok.com/es/city-ramallo/cate-other15/patient-safety-specialist-6414236775398512/","localIds":"332","cateId":null,"tid":null,"logParams":{"tid":"9d9a2c03-d0b4-4fc4-97c0-af920cf6114d","sid":"0c59db6e-ccfd-47af-ba35-aa24ab62678f"},"attrParams":{"summary":null,"highLight":["Supervisa programa de farmacovigilancia","Gestiona informes de eventos adversos","Apoya la experimentación clínica"],"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Tipo de empleo","value":"Tiempo completo","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Modalidad de trabajo","value":"Presencial","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Ramallo,Buenos Aires Province","unit":null}]},"addDate":1761112248077,"categoryName":"Otro","postCode":null,"secondCateCode":"healthcare-medical","kycTag":null,"pictureUrls":null,"isFavorite":false}],"localIds":"1,332","pageTitle":"Otro en Ramallo","topCateCode":"jobs","catePath":"4000,4182,4214","cateName":"Empleos,Salud y Medicina,Otro","breadCrumbSeo":{"type":"BreadcrumbList","itemListElement":[{"position":1,"name":"Casa","item":"https://ar.ok.com/es/city-ramallo/","@type":"ListItem"},{"position":2,"name":"Empleos","item":"https://ar.ok.com/es/city-ramallo/cate-jobs/","@type":"ListItem"},{"position":3,"name":"Salud y Medicina","item":"https://ar.ok.com/es/city-ramallo/cate-healthcare-medical/","@type":"ListItem"},{"position":4,"name":"Otro","item":"http://ar.ok.com/es/city-ramallo/cate-other15/","@type":"ListItem"}],"@type":"BreadcrumbList","@context":"https://schema.org"},"cateCode":"other15","total":4,"sortList":[{"sortName":"Mejor coincidencia","sortId":0},{"sortName":"Más reciente","sortId":1}],"breadCrumb":[{"name":"Casa","link":"https://ar.ok.com/es/city-ramallo/"},{"name":"Empleos","link":"https://ar.ok.com/es/city-ramallo/cate-jobs/"},{"name":"Salud y Medicina","link":"https://ar.ok.com/es/city-ramallo/cate-healthcare-medical/"},{"name":"Otro","link":null}],"tdk":{"type":"tdk","title":"Información de contratación de Otro en Ramallo - 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Ubicación:
Ramallo
Categoría:
Otro
Indeed
mozo/a o camarero/a
29/09/2025
### **mozo/a o camarero/a**
MARIA NAZARENA ALFONSO
atencion de clientes
SAN PEDRO, BUENOS AIRES
**Oferta**
----------
Vacantes
1
Disponibilidad horaria
Tiempo parcial
Salario
A Convenir
**Tareas a Realizar**
---------------------
Resumen del puesto
atencion de clientes
Principales tareas a realizar
atencion de clientes
Beneficios
Comedor en la empresa, Obra social / medicina para toda la familia, Otros
**Detalles**
------------
Lugar de Trabajo
BUENOS AIRES \- SAN PEDRO \- \- PELEGRINI 900
Disponibilidad
Tiempo parcial
Dias laborales
Viernes, Sábado, Domingo
Horario de Entrada y Salida
17:00
21:00
**Requisitos**
--------------
Experiencia Requerida
2 años
Estudios
Secundarios
Idiomas
* Inglés, conocimientos mínimos: Básico
Conocimientos informáticos
* informatica, conocimientos mínimos: Básico
Postularme
Volver

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina
Salario negociable
Indeed
ayudante de ventas de comercio minorista
14/10/2025
### **ayudante de ventas de comercio minorista**
CAMILA FRANGI
atencion al publico
SAN PEDRO, BUENOS AIRES
**Oferta**
----------
Vacantes
1
Disponibilidad horaria
Tiempo parcial
Salario
A Convenir
**Tareas a Realizar**
---------------------
Resumen del puesto
atencion al publico
Principales tareas a realizar
atencion al publico
Beneficios
Obra social / medicina para toda la familia
**Detalles**
------------
Lugar de Trabajo
BUENOS AIRES \- SAN PEDRO \- \- MITRE 1500
Disponibilidad
Tiempo parcial
Dias laborales
Lunes, Martes, Miércoles, Jueves, Viernes, Sábado
Horario de Entrada y Salida
16:30
20:30
**Requisitos**
--------------
Experiencia Requerida
No
Estudios
Secundarios
Postularme
Volver

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina
Salario negociable
Indeed
operador/a de máquina de control textil o revis...
08/11/2025
### **operador/a de máquina de control textil o revisador/a**
SP INNOVACION SAS
OPERARIO DE MAQUINA DE COSER EN TALLER TEXTIL
SAN PEDRO, BUENOS AIRES
**Oferta**
----------
Vacantes
1
Disponibilidad horaria
Tiempo completo
Salario
A Convenir
**Tareas a Realizar**
---------------------
Resumen del puesto
OPERARIO DE MAQUINA DE COSER EN TALLER TEXTIL
Principales tareas a realizar
OPERARIO DE MAQUINA DE COSER EN TALLER TEXTIL
Beneficios
Obra social / medicina para toda la familia
**Detalles**
------------
Lugar de Trabajo
BUENOS AIRES \- SAN PEDRO \- \- CHIVILCOY 2990
Disponibilidad
Tiempo completo
Dias laborales
Lunes, Martes, Miércoles, Jueves, Viernes
Horario de Entrada y Salida
06:00
14:00
**Requisitos**
--------------
Experiencia Requerida
No
Estudios
Secundarios
Postularme
Volver

Güemes 2040, B2930 San Pedro, Provincia de Buenos Aires, Argentina
Salario negociable

Indeed
Especialista en Seguridad del Paciente
### **Resumen**
Supervisa y controla el programa de vigilancia de medicamentos, biológicos o dispositivos médicos de la empresa, incluyendo la recepción, evaluación, procesamiento y seguimiento de los informes de reacciones adversas. Participa en la resolución de cualquier responsabilidad legal y en el cumplimiento de las normativas gubernamentales. Garantiza una recepción, mantenimiento y evaluación precisos respecto al etiquetado del producto. Informa sobre eventos o reacciones según lo requieran las agencias reguladoras, incluyendo datos de eventos adversos procedentes de estudios clínicos, fuentes espontáneas o solicitadas, informes periódicos y de experiencia. Puede proporcionar detección y evaluación de señales de tendencia y seguridad. Apoya todas las actividades de experimentación clínica y postcomercialización.
### **Acerca del puesto**
Principales responsabilidades
\~ Apoyar la gestión de los procesos operativos para garantizar el cumplimiento de los procedimientos globales/locales de Novartis, así como de las normativas/normas/guías nacionales e internacionales sobre farmacovigilancia de productos comerciales e investigacionales de Novartis
\~ Gestionar la recopilación, el procesamiento, la documentación, la notificación y el seguimiento de todos los informes de eventos adversos (AE) para todos los productos Novartis provenientes de estudios clínicos, estudios postcomercialización (PMS), programas orientados al paciente (POP), registros y todos los informes espontáneos (SR).
\~ Transcribir, traducir (cuando sea necesario) e introducir con precisión y coherencia los datos de todos los eventos adversos graves (de estudios clínicos) y de todos los eventos adversos (de POP, PMS, registros y todos los SR) desde los documentos originales a los sistemas de seguridad, haciendo hincapié en la puntualidad y calidad.
\~ Registrar y hacer seguimiento de la recepción, envío y distribución de documentos como SAE, SR, notificaciones de investigadores, etc., en colaboración con otros departamentos
\~ Gestionar la notificación/envío/distribución de informes/actualizaciones/información de seguridad a las Autoridades Sanitarias Locales y/o a las operaciones clínicas, en colaboración con otros departamentos.
\~ Colaborar con otros asociados de fotovoltaica locales/globales para garantizar una evaluación precisa de los datos de seguridad.
\~ Interactuar e intercambiar información de seguridad relevante con LHA, asociados de fotovoltaica, otros grupos funcionales y contratistas de terceros, si corresponde.
\~ Detectar y monitorear las normativas globales/regional/nacionales (casuales) sobre farmacovigilancia y proporcionar actualizaciones a la organización global de PVO.
\~ Desarrollar, actualizar e implementar procedimientos locales para garantizar el cumplimiento de los procedimientos globales de PVO y los requisitos nacionales.
\~ Gestión y mantenimiento de todas las bases de datos PVO asignadas pertinentes, si corresponde.
\~ Desarrollar y actualizar materiales de formación para farmacovigilancia
\~ Garantizar el apoyo y cierre de auditorías, actividades del plan de acción correctiva y visitas de inspección de la autoridad sanitaria.
\~ Proporcionar información oportuna y pertinente a coordinadores de ensayos, AGENCIAS y otro personal de Novartis
\~ Distribución de muestras promocionales (si corresponde)
Indicadores clave de rendimiento
Supervisa y controla el programa de vigilancia de medicamentos, biológicos o dispositivos médicos de la empresa, incluyendo la recepción, evaluación, procesamiento y seguimiento de los informes de reacciones adversas. Participa en la resolución de cualquier responsabilidad legal y en el cumplimiento de las normativas gubernamentales. Garantiza una recepción, mantenimiento y evaluación precisos respecto al etiquetado del producto. Informa sobre eventos o reacciones según lo requieran las agencias reguladoras, incluyendo datos de eventos adversos procedentes de estudios clínicos, fuentes espontáneas o solicitadas, informes periódicos y de experiencia. Puede proporcionar detección y evaluación de señales de tendencia y seguridad. Apoya todas las actividades de experimentación clínica y postcomercialización.
Experiencia laboral
\~ Gestión y ejecución de operaciones
\~ Colaboración interempresarial
\~ Extensión funcional
Habilidades
\~ Archivado (documentos)
\~ Farmacovigilancia
\~ Ciencia de la seguridad
\~ Bases de datos
\~ Formación de empleados
\~ Crónica
Idioma
Inglés
**Por qué Novartis:** Ayudar a las personas que padecen enfermedades y a sus familias requiere más que ciencia innovadora. Requiere una comunidad de personas inteligentes y apasionadas como tú. Colaborando, apoyándose e inspirándose mutuamente. Unidos para lograr avances que transformen la vida de los pacientes. ¿Listo para crear un futuro mejor juntos? https://www.novartis.com/about/strategy/people\-and\-culture
**Únete a nuestra red de Novartis:** ¿No es este el puesto adecuado en Novartis para ti? Regístrate en nuestra comunidad de talentos para mantenerte conectado y conocer oportunidades profesionales adecuadas tan pronto como surjan: https://talentnetwork.novartis.com/network
**Beneficios y recompensas:** Consulta nuestro manual para conocer todas las formas en que te ayudaremos a prosperar personal y profesionalmente: https://www.novartis.com/careers/benefits\-rewards
División
Desarrollo
Unidad de negocio
Medicamentos Innovadores
Ubicación
Argentina
Sitio
Ramallo (Argentina)
Empresa / Entidad Legal
AR01 (FCRS \= AR001\) Novartis Argentina S.A.
Área Funcional
Investigación \& Desarrollo
Tipo de trabajo
Tiempo parcial
Tipo de empleo
Regular
Trabajo por turnos
No

GXCH+HM Ramallo, Buenos Aires Province, Argentina
Salario negociable
Puestos populares
Ciudades populares