Trabajo regulatory en San Miguel

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...

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...

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. -...

KARL STORZ is a global leader in minimally invasive surgery and endoscopic innovation, founded in 1945 and headquartered in Tuttlingen, Germany. The company is recognized worldwide for pioneering rigid endoscopy and advancing cutting‑edge imaging and surgical technologies used across multiple medical specialties. We are hiring Regulatory Affairs & Quality Specialist – Chile We are looking for...

Job Description Garantizar el cumplimiento normativo y la obtención/mantenimiento oportuno de los registros sanitarios y autorizaciones regulatorias de medicamentos veterinarios, asegurando la conformidad técnica y documental a lo largo del ciclo de vida del producto y habilitando el acceso a Chile. Responsabilidades - Punto contacto de regulatorio para Chile en Salud Animal (CORA) para...

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...

Why should you join dLocal? dLocal enables the biggest companies in the world to collect payments in 40 countries in emerging markets. Global brands rely on us to increase conversion rates and simplify payment expansion effortlessly. As both a payments processor and a merchant of record where we operate, we make it possible for our merchants to make inroads into the world's fastest-growing,...

Job Description The Legal Entity Control team is responsible for financial, capital adequacy and liquidity oversight of their legal entity, and is tasked with ensuring that a strong control environment exists as it relates to all businesses, products and operational areas that impact the Legal Entity financials and regulatory reporting of the firm. Responsibilities This role provides an...

2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Why should you join dLocal? dLocal enables the biggest companies in the world to collect payments in 40 countries in emerging markets. Global brands rely on us to increase conversion rates and simplify payment expansion effortlessly. As both a payments processor and a merchant of record...

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 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...

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 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...

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...