Join to apply for the quality assurance specialist role at merck healthcare join to apply for the quality assurance specialist role at merck healthcare work your magic with us! ready to explore, break barriers, and discover more? we know you’ve got big plans – so do we! our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in healthcare, life science, and electronics. together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. that's why we are always looking for curious minds that see themselves imagining the unimaginable with us. united as one for patients, our purpose in healthcare is to help create, improve and prolong lives. we develop medicines, intelligent devices and innovative technologies in therapeutic areas such as oncology, neurology and fertility. our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. joining our healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. your role you will be responsible for ensuring compliance with regulatory standards and global quality standards in colombia and ecuador, aligned with gmp, gdp guidelines, and local regulations, including pharmacovigilance and medical devices. you will support the quality assurance manager in the effective execution and continuous improvement of the quality managem...
Your role you will be responsible for ensuring compliance with regulatory standards and global quality standards in colombia and ecuador, aligned with gmp, gdp guidelines, and local regulations, including pharmacovigilance and medical devices. you will support the quality assurance manager in the effective execution and continuous improvement of the quality management system, in line with the global strategy of healthcare operations. you will manage the process of complaints, deviations, and change controls, ensure the release of pharmaceutical products, coordinate medical device inspections, and provide support during audits. you will also act as the key user of sap (quality module), leading training, change testing, and ticket follow-ups. this role requires constant communication with local and global teams, analytical thinking, and a strong results orientation in a technical and multicultural environment. who you are - intermediate-high english (ability to read guidelines, interact in global calls, and generate reports in technical english) - degree in pharmaceutical chemistry. - current registration and professional license with invima. - experience in the pharmaceutical industry, in areas such as quality, product release, pharmacovigilance, and gmp/gdp compliance. - knowledge of resolution 4816 of 2008 (pharmacovigilance), invima guidelines, who guidelines, and gxp regulations. - desirable: training as an internal auditor and experience with systems such as trackwise, sap (le/wm), mango, excel, and sharepoint. - familiarity with validation processes, documen...
Your role you will be responsible for ensuring compliance with regulatory standards and global quality standards in colombia and ecuador, aligned with gmp, gdp guidelines, and local regulations, including pharmacovigilance and medical devices. you will support the quality assurance manager in the effective execution and continuous improvement of the quality management system, in line with the global strategy of healthcare operations. you will manage the process of complaints, deviations, and change controls, ensure the release of pharmaceutical products, coordinate medical device inspections, and provide support during audits. you will also act as the key user of sap (quality module), leading training, change testing, and ticket follow-ups. this role requires constant communication with local and global teams, analytical thinking, and a strong results orientation in a technical and multicultural environment. who you are - intermediate-high english (ability to read guidelines, interact in global calls, and generate reports in technical english) - degree in pharmaceutical chemistry. - current registration and professional license with invima. - experience in the pharmaceutical industry, in areas such as quality, product release, pharmacovigilance, and gmp/gdp compliance. - knowledge of resolution 4816 of 2008 (pharmacovigilance), invima guidelines, who guidelines, and gxp regulations. - desirable: training as an internal auditor and experience with systems such as trackwise, sap (le/wm), mango, excel, and sharepoint. - familiarity with validation processes, document manage...
Your role you will be responsible for ensuring compliance with regulatory standards and global quality standards in colombia and ecuador, aligned with gmp, gdp guidelines, and local regulations, including pharmacovigilance and medical devices. you will support the quality assurance manager in the effective execution and continuous improvement of the quality management system, in line with the global strategy of healthcare operations. you will manage the process of complaints, deviations, and change controls, ensure the release of pharmaceutical products, coordinate medical device inspections, and provide support during audits. you will also act as the key user of sap (quality module), leading training, change testing, and ticket follow-ups. this role requires constant communication with local and global teams, analytical thinking, and a strong results orientation in a technical and multicultural environment. who you are intermediate-high english (ability to read guidelines, interact in global calls, and generate reports in technical english) degree in pharmaceutical chemistry. current registration and professional license with invima. experience in the pharmaceutical industry, in areas such as quality, product release, pharmacovigilance, and gmp/gdp compliance. knowledge of resolution 4816 of 2008 (pharmacovigilance), invima guidelines, who guidelines, and gxp regulations. desirable: training as an internal auditor and experience with systems such as trackwise, sap (le/wm), mango, excel, and sharepoint. familiarity with validation processes, document management, and a...
Your role you will be responsible for ensuring compliance with regulatory standards and global quality standards in colombia and ecuador, aligned with gmp, gdp guidelines, and local regulations, including pharmacovigilance and medical devices. you will support the quality assurance manager in the effective execution and continuous improvement of the quality management system, in line with the global strategy of healthcare operations. you will manage the process of complaints, deviations, and change controls, ensure the release of pharmaceutical products, coordinate medical device inspections, and provide support during audits. you will also act as the key user of sap (quality module), leading training, change testing, and ticket follow-ups. this role requires constant communication with local and global teams, analytical thinking, and a strong results orientation in a technical and multicultural environment. who you are intermediate-high english (ability to read guidelines, interact in global calls, and generate reports in technical english)degree in pharmaceutical chemistry.current registration and professional license with invima.experience in the pharmaceutical industry, in areas such as quality, product release, pharmacovigilance, and gmp/gdp compliance.knowledge of resolution 4816 of 2008 (pharmacovigilance), invima guidelines, who guidelines, and gxp regulations.desirable: training as an internal auditor and experience with systems such as trackwise, sap (le/wm), mango, excel, and sharepoint.familiarity with validation processes, document management, and activit...
Buscamos un desarrollador de software fullstack remoto senior con más de 5 años de experiência desarrollando software en tecnologías definidas o relacionadas para unirse a nuestro equipo en crecimiento. somos una empresa de tecnología con una estrategia global de organic enterprise system, que es un poderoso ecosistema de aplicaciones y componentes escalables en la nube que respalda negocios, procesos, flujos de trabajo empresariales, informes inteligentes, administración de medios inteligentes y análisis de datos avanzados a través de tecnologías predictivas de ia. esta es una posición remota y aceptamos solicitudes desde cualquier lugar de colombia funciones del cargo: poder identificar y solucionar vulnerabilidades y problemas de seguridad. poder crear modelos relacionales normalizados. entender el funcionamiento del software para poder cumplir los requerimientos del cliente y lograr una mejor satisfacción con el servicio. escribir y ejecutar pruebas unitarias de calidad. comprender los procesos automatizados para construir una aplicación, probarla y documentarla. requerimientos del cargo: 5+ años como desarrollador full stack (angular, ionic, typescript) habilidad experta en python, node.js. experiência con git. experiência con bases de datos nosql, idealmente dynamodb. conocimientos en bases de datos de grafos como neo4j. opcionalmente, experiência con arquitectura sin servidor (aws). opcionalmente, experiência con firebase database. excelentes habilidades de comunicación. nível de inglés escrito - b1. opcionales: inteligencia artificial, blockchai...
Funciones del cargo poder identificar y solucionar vulnerabilidades y problemas de seguridad. poder crear modelos relacionales normalizados. entender el funcionamiento del software para poder cumplir los requerimientos del cliente y lograr una mejor satisfacción con el servicio. escribir y ejecutar pruebas unitarias de calidad. comprender los procesos automatizados para construir una aplicación, probarla y documentarla. 3+ años como desarrollador full stack (angular, ionic, typescript) como desarrollador full stack (angular, ionic, typescript) habilidad experta en python, node.js. experiencia con git. experiencia con bases de datos nosql, idealmente dynamodb. conocimientos en bases de datos de gráficos como neo4j. opcionalmente, experiencia con arquitectura sin servidor (aws). opcionalmente, experiencia con firebase database. excelentes habilidades de comunicación. nivel de inglés escrito - b1....
Buscamos un **desarrollador de software fullstack remoto senior** con más de 5 años de experiência desarrollando software en tecnologías definidas o relacionadas para unirse a nuestro equipo en crecimiento. somos una empresa de tecnología con una estrategia global de organic enterprise system, que es un poderoso ecosistema de aplicaciones y componentes escalables en la nube que respalda negocios, procesos, flujos de trabajo empresariales, informes inteligentes, administración de medios inteligentes y análisis de datos avanzados a través de tecnologías predictivas de ia. esta es una posición remota y aceptamos solicitudes desde cualquier lugar de colombia **funciones del cargo**: - poder identificar y solucionar vulnerabilidades y problemas de seguridad. - poder crear modelos relacionales normalizados. - entender el funcionamiento del software para poder cumplir los requerimientos del cliente y lograr una mejor satisfacción con el servicio. - escribir y ejecutar pruebas unitarias de calidad. - comprender los procesos automatizados para construir una aplicación, probarla y documentarla. **requerimientos del cargo**: - 5+ años como desarrollador full stack (angular, ionic, typescript) - habilidad experta en python, node.js. - experiência con git. - experiência con bases de datos nosql, idealmente dynamodb. - conocimientos en bases de datos de grafos como neo4j. - opcionalmente, experiência con arquitectura sin servidor (aws). - opcionalmente, experiência con firebase database. - excelentes habilidades de comunicación. - nível de inglés escrito - b1. **opcion...
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