Trabajo de regulatory en Puente Alto

A leading clinical research organization in Chile is seeking a Regulatory Submissions Coordinator to support various regulatory projects. The ideal candidate will have a bachelor's degree in Life Sciences and at least 3–4 years of experience in regulatory submissions. Responsibilities include providing daily project support, conducting quality control of documents, and advising team members on...

Overview ¡Únete a nuestro equipo en Tervis Pharma!, como Regulatory Affairs Specialist. ¿Te apasiona el mundo farmacéutico y quieres ser parte de una compañía que trabaja con altos estándares de calidad y ética? En Tervis Pharma (que pertenece a grupo Nutraline/All Nutrition) buscamos un Regulatory Affairs Specialist, que nos ayude a garantizar el cumplimiento normativo y a mantener nuestra...

Tervis---### Detalles de la ofertaVacantes1Horas Semanales42.0JornadaCompletaÁreaGerencia Comercial Tervis## Más información¡Somos Grupo Nutraline – All Nutrition! Un ecosistema de empresas jóvenes, dinámicas y con un fuerte ADN emprendedor.Nuestro propósito es claro: brindamos bienestar y calidad de vida. Nos mueve la nutrición, la innovación y el compromiso de ofrecer experiencias y asesorías...

Your Tasks - Integrarte al equipo de Regulatory Affairs. - Revisión de documentación técnica. - Compilación de expedientes para el registro de productos. - Verificación de que los documentos cumplan con los requisitos de Argentina y Chile. - Organización y actualización de bases de datos regulatorias. - Asistencia en auditorías internas o externas relacionadas con cumplimiento regulatorio. -...

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We are seeking an Accounting and Regulatory Reporting Analyst for our team based in Santiago , of which the descriptions are as follows: Supporting key tasks related to accounting and regulatory reporting, including but not limited to: preparing, analyzing and maintaining accounting balances; ensuring accurate registration and mapping of transactions in the systems; producing timely and reliable...

Description Senior Consultant Regulatory Intelligence (Portugal or Serbia based) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to...

Department: Language Services Specialization: Regulatory Submissions (Marketing Authorization) Location: Hybrid (Argentina, Latam and/or Canada) Employment Type: Full time Role Purpose As part of IQVIA's Project Management team, you will coordinate and manage the full lifecycle of Regulatory Submissions translation and localization projects for Marketing Authorization, ensuring IQVIA's...

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Una empresa internacional de cuidado personal busca un nuevo integrante para su equipo de Regulatory Affairs en Santiago, Chile. Las responsabilidades incluyen la revisión de documentación técnica y la organización de bases de datos regulatorias. Se buscan candidatos con habilidades sólidas en Excel y Power BI, que sean proactivos y estén dispuestos a aprender en un entorno colaborativo y...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

Una empresa farmacéutica considerada busca un Regulatory Affairs Specialist para asegurar que las operaciones cumplan con las regulaciones locales e internacionales. Serás el pilar en la gestión de documentos y permisos regulatorios. Se requieren al menos 3 años de experiencia en el sector, así como un título en Química y Farmacia. Las competencias clave incluyen trabajo en equipo, orientación al...

Únete a nuestro equipo en Tervis Pharma, como Regulatory Affairs Specialist ¿Te apasiona el mundo farmacéutico y quieres ser parte de una compañía que trabaja con altos estándares de calidad y ética? En Tervis Pharma (que pertenece a grupo Nutraline/All Nutrition) buscamos un Regulatory Affairs Specialist, que nos ayude a garantizar el cumplimiento normativo y a mantener nuestra reputación como...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

A leading clinical research organization in Chile is seeking a Regulatory Submissions Coordinator to support various regulatory projects. The ideal candidate will have a bachelor's degree in Life Sciences and at least 3–4 years of experience in regulatory submissions. Responsibilities include providing daily project support, conducting quality control of documents, and advising team members on...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...

A leading clinical research organization is seeking a full-time, remote Regulatory Submissions Manager to join their Study Start Up team in Chile. This role involves managing global start-up activities, performing quality checks on submission documents, and preparing informed consent forms. Candidates should have at least 4 years of related experience, strong communication skills, and a...