Trabajo Regulatory Affairs Analyst en Comunidad de Madrid

Taketalent is partnering with PharmaMar, a leading biopharmaceutical company dedicated to the research, development, and production of innovative oncology therapies, to find a Regulatory Affairs Project Manager with an international scope. This is a hybrid position, ideal for professionals eager to manage strategic regulatory projects globally and contribute to the success of end-to-end...

We're seeking a detail-oriented and proactive Senior Regulatory Associate to support the preparation and submission of high-quality regulatory documentation. This is a fantastic opportunity for professionals with 1-3 years of experience in Regulatory Affairs who are ready to take the next step in their career. Key Responsibilities: - Publish, dispatch, and archive regulatory submissions in...

Job Title: European Regulatory Affairs Manager Location: Madrid, Spain - Hybrid Remuneration: Competitive salary and package Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the small...

Associate Regulatory Affairs Director – IQVIA We are seeking a highly skilled and detail‑oriented Associate Director of Regulatory Affairs to lead clinical documentation and regulatory submission activities in support of EU MDR compliance. In this strategic role, you will oversee the preparation, finalization, and lifecycle management of clinical and regulatory documents for services across the...

Overview Join to apply for the Operations Manager (Regulatory Affairs) role at Revolut.About Revolut: People deserve more from their money. More visibility, more control, and more freedom. Since 2015, Revolut has been on a mission to deliver just that. Our powerhouse of products—including spending, saving, investing, exchanging, travelling, and more—help our 60+ million customers get more from...

Desde Paul Marlex estamos colaborando con una empresa industrial del sector alimentación, que precisa incorporar un / a Regulatory Affairs para su equipo de Calidad, en dependencia directa de la Quality Manager. ¿Cuál será tu misión en la empresa? Responsabilidades - Control de requisitos legales / regulatorios de los productos. - Definición y realización de fichas técnicas y especificaciones...

Work Flexibility Work Flexibility : Hybrid Location Location : Madrid Spain Contract Type Contract Type : Temporary 10 months (until september 2026) Department Department : RAQA About the Role About the Role : Are you ready to launch your career in Regulatory Affairs and Quality Assurance within a dynamic international environment Were looking for a motivated and detail-oriented RA /...

LIVISTO es una empresa Farmacéutica Internacional con una amplia experiencia en el sector veterinario, dedicada al desarrollo, producción y comercialización de productos de alta calidad para la salud animal, destinados a la ganadería y avicultura, así como a animales de compañía y caballos. El grupo LIVISTO, con más de 500 empleados, opera en más de 125 países. ¿Te unes a nosotros /...

Estamos buscando un / a Junior Regulatory Affairs Specialist para unirse a nuestro equipo en pleno crecimiento en el sector dermocosmético médico-estético. Este puesto combina funciones de Regulatory Affairs, Garantía de Calidad, siendo clave para el desarrollo y expansión internacional de la empresa. Si eres una persona joven, motivada, con ganas de aprender y trabajar en un entorno dinámico y...

Senior Regulatory Affairs Specialist BD is one of the largest global medical technology companies. The Senior Regulatory Affairs Specialist will ensure regulatory compliance of products and services for assigned countries (France – Eybens (38) or Spain – San Agustin del Guadalix), maintain alignment with authorities, customers, and internal stakeholders, contribute to strategic regulatory...

Regulatory Affairs Study Start Up Specialist II (RASSU) - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. - Prepare and QC Clinical Trial Application forms (via CTIS or...

Desde ManpowerGroup Talent Solutions estamos buscando un / a Regulatory Affairs Specialist Row para el Área de B2B de una multinacional farmacéutica referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Tu misión dentro del departamento consistirá en ayudar a la expansión internacional del B2B en los mercados de LATAM, MENA, Sud-este Asiático, Australia, Israel,...

Regulatory Affairs Study Start Up Specialist II (RASSU) Join to apply for the Regulatory Affairs Study Start Up Specialist II (RASSU) role at CTI Clinical Trial and Consulting Services What You’ll Do - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in...

Da el primer paso hacia tu futuro profesional en Laboratorios Ordesa : tu talento suma, nuestra pasión por la salud nos une. ¿Todavía no sabes quiénes somos? Déjanos presentarnos… Laboratorios Ordesa es una compañía referente en el sector de la nutrición especializada, con una sólida trayectoria y en pleno crecimiento. Apostamos por la innovación, el rigor científico y el compromiso con la...

Company Description Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution...

Regulatory Affairs & Product Development Specialist Barcelona - Modalidad híbrida ¿Te apasiona el desarrollo y la transferencia tecnológica de productos farmacéuticos? ¿Buscas un rol técnico con proyección y contacto internacional, donde combinar la gestión regulatoria con la coordinación de proyectos estratégicos? Estamos buscando un / a Specialist en Asuntos Regulatorios y Desarrollo de...

Job DescriptionThe PositionCoordinating and supporting all regulatory activities to maintain registrations and to obtain new marketing authorisations for the company portfolio/pipeline subject to EU procedures (Centralised, Mutual Recognition, Decentralised, National authorised Procedures) across therapeutic areas. The position also requires strong project management skills to oversee regulatory...

Taketalent is partnering with PharmaMar , a leading biopharmaceutical company dedicated to the research, development, and production of innovative oncology therapies , to find a Regulatory Affairs Project Manager with an international scope . This is a hybrid position , ideal for professionals eager to manage strategic regulatory projects globally and contribute to the success of end-to-end...

We're seeking a detail-oriented and proactive Senior Regulatory Associate to support the preparation and submission of high-quality regulatory documentation. This is a fantastic opportunity for professionals with 1-3 years of experience in Regulatory Affairs who are ready to take the next step in their career. Key Responsibilities: - Publish, dispatch, and archive regulatory submissions in...

1 Year (FREELANCE) Contract Opportunity: EU Regulatory Affairs - Senior Manager (Biotech) A leading biotechnology company is seeking a highly experienced EU Regulatory Affairs Senior Manager to support development-stage projects and initial Marketing Authorisation Applications (MAAs) across Europe. Key Responsibilities Lead and support EU Clinical Trial Authorisation (CTA) submissions and...