Trabajo de Regulatory Affairs en Galicia

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

A prominent medical technology company in San Agustín del Guadalix is seeking a Regulatory Affairs Trainee to support the EMEA team with GTM activities in Spain and Portugal. Responsibilities include handling product notifications and assisting with CE mark activities and international registrations. Candidates must have a university degree in Life or Engineering Science or equivalent, and an...

OverviewJob Description SummaryAs Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team.Job DescriptionMain responsibilities include:GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customersBD, SA...

En pocas palabras Posición: Regulatory Affairs Associate - International Markets Localización: Azuqueca de Henares Experiencia: al menos 3-4 años en funciones similares ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama...

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France (Eybens) or Spain (San Agustin Del Guadalix). You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, and internal stakeholders. You will contribute to strategic regulatory analysis,...

Registro de Medicamentos y Productos Sanitarios | Industria Farmacéutica Tu nueva empresa Reconocido Laboratorio Farmacéutico con presencia nacional e internacional. Tu nuevo puesto Seleccionamos profesional con experiencia en Asuntos Regulatorios para dar soporte en la gestión de expedientes técnicos de medicamentos y productos sanitarios, garantizando su cumplimiento normativo y apoyando el...

Somos un grupo internacional innovador, con amplia experiencia en la comercialización de productos farmacéuticos en el ámbito geográfico de Centroamérica y el Caribe. Objetivo principal del puesto: Gestionar los registros sanitarios de los diferentes productos comercializados en el territorio donde opera el Grupo ya sean medicamentos, producto cosmético, producto natural, suplemento alimenticio...

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Visits will be scheduled well in advance. Study Overview - Study Duration: 20 months - Visit Duration: Approximately 2 hours per visit Key Responsibilities -...

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years...

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Perform clinical trial-related procedures including blood sampling and injections ECG performance (recording only; Qualified nurse with a minimum of 3 years...

OverviewJob Description SummaryAs Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team.Job DescriptionMain responsibilities include:GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customersBD, SA...

Overview As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team.Main responsibilities GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customersBD, SA manufacturer: CE mark activity, international...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

A prominent medical technology company in San Agustín del Guadalix is seeking a Regulatory Affairs Trainee to support the EMEA team with GTM activities in Spain and Portugal. Responsibilities include handling product notifications and assisting with CE mark activities and international registrations. Candidates must have a university degree in Life or Engineering Science or equivalent, and an...

En pocas palabras Posición: Regulatory Affairs Associate - International Markets Localización: Azuqueca de Henares Experiencia: al menos 3-4 años en funciones similares ¿Quieres saber más? INSUD PHARMA opera en toda la cadena de valor farmacéutica, aportando conocimientos especializados y experiencia en investigación científica, desarrollo, fabricación, venta y comercialización de una amplia gama...

A leading global medical technology company is seeking a Regulatory Affairs Trainee in San Agustín del Guadalix, Spain. The role involves supporting GTM activities and coordinating with national authorities, along with managing product notifications and audits. Candidates should possess a university degree related to Life or Engineering Science and hold an internship agreement with their...

A leading global medical technology company is seeking a Regulatory Affairs Trainee in San Agustín del Guadalix, Spain. The role involves supporting GTM activities and coordinating with national authorities, along with managing product notifications and audits. Candidates should possess a university degree related to Life or Engineering Science and hold an internship agreement with their...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

Overview As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team.Main responsibilities GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customersBD, SA manufacturer: CE mark activity, international...