Trabajo de Regulatory Affairs en Madrid

Senior Regulatory Affairs Technician (Pozuelo, Madrid) ¿Tienes experiencia en Regulatory Affairs en medical devices, cosmética o farma? ¿Buscas un nuevo reto en un entorno altamente regulado y en plena transformación? En Laboratorios Indas buscamos un/a Senior Regulatory Affairs Technician para nuestro equipo en Pozuelo (Madrid). La persona seleccionada convivirá durante 6 meses con el/la...

Job Title: Regulatory Affairs Specialist Spain Full Time Permanent Location: Spain (Madrid) About Novumgen Novumgen is a rapidly expanding, science-driven pharmaceutical company committed to delivering high-quality, accessible medicines across global markets. Our diverse portfolio spans specialty generics, complex formulations, and innovative therapeutic solutions. With a strong focus on...

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional...

Overview Are you motivated by shaping medical, regulatory, quality, pharmacovigilance and clinical strategies that impact patients across countries? In this leadership role, you will drive the Medical & Regulatory Affairs agenda for Spain and Portugal, working cross-functionally and externally with key stakeholders to secure optimal support for Lundbeck’s products throughout their...

When our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross‑functional teams. The role can...

🔍 Senior Consultant Regulatory Affairs 📍 Location: Hybrid-Spain 🕓 Type: Full-time QbD Group offersknowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distributionfor companies active in Pharma, Biotech and Medical Devices/IVD. Our Regulatory Affairs division supports customers throughout theentire regulatory lifecycleof their products,...

Job Function Regulatory Affairs Group Job Sub Function Regulatory Affairs Job Category Professional All Job Posting Locations Beerse, Antwerp, Belgium; Leiden, South Holland, Netherlands; Madrid, Spain; Warsaw, Masovian, Poland About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex...

Regulatory Affairs Specialist - Group Leader - Crop Protection - Full-time Eurofins Scientific is an international life sciences company that offers customers from various industries a unique range of analytical services to make life and our environment safer, healthier and more sustainable. From the food you eat to the water you drink to the medicines you rely on, Eurofins works with the...

Position Summary The Regulatory Affairs Specialist is responsible for identifying and obtaining scientific, engineering, and regulatory information for review, preparation, and maintenance of technical documentation for submission to regulatory authorities in the countries/regions where the company wishes to market medical products. This position works with the regulatory authorities, or with...

MFC-2510-344 REGULATORY AFFAIRS MANAGER MADRID Overall responsibilities - To provide regulatory advice and support to the organisation on the content of existing marketing authorisations and for products in development phase. - To provide general regulatory advice and support to other departments. - Review and approval of promotional and non-promotional material to comply with local...

Job Title: Regulatory Affairs Specialist Spain Full Time Permanent Location: Spain (Madrid) Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora. About Novumgen Novumgen is a rapidly expanding, science-driven pharmaceutical company committed to delivering high-quality, accessible medicines across global...

Sateliot is a Barcelona-based Startup in the New Space sector, becoming the first satellite telecommunications operator that will provide global and continuous connectivity to all the elements that will make up the massive Internet of Things IoT) universe under the 5G protocol . YOUR MISSION You will play an integral role in ensuring Sateliot’s compliance with regulatory requirements...

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...

Overview Location: Barcelona, Spain Opella is the self-care challenger with a broad portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market. Our mission is to bring health in people’s hands by making self-care simple for over half a billion consumers. Headquartered in France, Opella is the maker of well-known brands and operates with a global team and multiple...

Digital Lead for Medical, Regulatory Affairs & Pharmacovigilance Platforms Location : Barcelona, Spain Opella is the self‑care challenger with the purest and third‑largest portfolio in the Over‑The‑Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally. Our mission : to bring health in people’s hands by making self‑care as simple as it should be for over half a billion consumers...

Un grupo sanitario líder en España busca un/a Técnico/a de Regulatory Affairs para el Hospital Universitario Quirónsalud en Madrid. El candidato facilitará el flujo de documentos para ensayos clínicos y tendrá responsabilidades como organizar reuniones y mantener la documentación actualizada. Se requiere una licenciatura en Ciencias y al menos 6 meses de experiencia en un puesto similar....

Environmental Resources Management (ERM) is seeking an experienced Plant Protection Regulatory Affairs professional to join us as a Project Manager in Southern Europe. This is a great opportunity to join a global consultancy with a strong track record of advising clients in the chemical sector, with a focus on agrochemicals, biocides and REACH, to help them navigate the complexities of the EU...

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...

Senior Regulatory Affairs Technician (Pozuelo, Madrid) ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. ¿Tienes experiencia en Regulatory Affairs en medical devices, cosmética o farma? ¿Buscas un nuevo reto en un entorno altamente regulado y en plena transformación? En Laboratorios Indas buscamos un/a Senior...

A leading consulting firm is seeking a Senior Consultant in Regulatory Affairs to manage complex projects and provide high-quality regulatory consulting services. The ideal candidate will have significant regulatory affairs experience, including a successful track record in the development and lifecycle maintenance of medicinal products. This role offers an attractive salary package, job...