Trabajo de Regulatory Affairs Analyst en 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 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,...

Experience HELM as a unique family business and an attractive employer. Through a constant exchange with all stakeholders, our goal is to offer our customers future-oriented solutions. The Business Unit Crop Solutions Europe is one of the leading marketing (distribution) organizations with a wide range of high-quality products in the field of fertilizers and biostimulation. Crop Solutions Europe...

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...

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 Title: Regulatory Affairs Manager Europe Location: Barcelona, Spain (Onsite) Department: Regulatory / Pharmacovigilance Employment Type: Full-Time, Permanent Industry: Pharmaceuticals About Vivanta Generics MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, the company has 17 API and 8...

When our values align, there's no limit to what we can achieve. Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented Regulatory Affairs Consultant to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations. As the Regulatory Affairs Consultant you will...

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 /...

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...

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...

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...

Overview Our team members are at the heart of everything we do. At Cencora we are united in our responsibility to create healthier futures and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Cencora...

Job Title: European Regulatory Affairs Manager Location: Madrid, Spain - Hybrid 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 team and lead several Regulatory Affairs...

Job Title: European Regulatory Affairs Manager Location: Madrid, Spain - Hybrid 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 team and lead several Regulatory Affairs...