Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription
Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction: The Associate Director,Patient Safety Scientist role works collaboratively with the Global Safety Physician (GSP) and (Senior/Principal) PV Scientist with
Director, Principal Patient Safety Scientist Oncology Location: Barcelona, Spain (on-site) 3 days working from the office and 2 days working from home. AstraZeneca is a global, science‑led, patient‑focused biopharmaceutical company that focuses on the discovery, development
Position SummaryThe Medical Safety Director, Clinical Scientist provides clinical science support to product activities, ensuring high-quality clinical input into routine maintenance documentation, safety and labeling deliverables, and issue resolution activities.This role partners closely with cross-functional product
Be part of the future of drug safety at Asphalion! We’re looking for a Drug Safety Senior Officer ready to embrace new challenges in a fast-moving, international environment. If you thrive on precision and want to
# Manager Risk ManagementREQ- Jul 28, 2026SpainAvailable in:English# SummaryReady to make a direct impact on patient safety across the globe? At Novartis, every decision we make is driven by our purpose to reimagine medicine for patients.
Be part of the future of drug safety at Asphalion! We’re looking for a Drug Safety Senior Officer ready to embrace new challenges in a fast-moving, international environment. If you thrive on precision and want to
We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.Our purpose is simple: to transform patients’ lives
En ALTEN tenemos claro que el éxito de nuestros proyectos se debe a las personas que forman nuestro equipo. Si eres médico/a con experiencia en farmacovigilancia y buscas un proyecto estratégico dentro de una compañía farmacéutica
Overview In this role you will provide medical leadership for patient safety across clinical development and post-marketing for assigned products. You will oversee medical review, signal detection/management, and benefit–risk assessment in line with global regulations, partnering
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join
NESA WORLD · Donostia-San Sebastián En NESA WORLD diseñamos, fabricamos y comercializamos dispositivos médicos de neuromodulación no invasiva (Clase IIa, MDR 2017/745). Nuestra tecnología está presente en más de 47 países. Buscamos incorporar un/a Regulatory Affairs
Overview In this role you will lead safety science for complex oncology products, shaping proactive pharmacovigilance and risk management across development stages. You work closely with cross-functional teams to deliver safety strategies, regulatory documents, and submissions
Overview In this role you will lead safety and risk management activities for assigned clinical development programs or marketed products, ensuring safe and effective use for patients and healthcare providers. You will drive safety strategy, contribute
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join
Overview In this role you will lead pharmacovigilance and risk management for designated products, collaborating with the Global Safety Physician and PV scientists. You will author safety documents, provide PV input for regulatory reports, and lead
En ALTEN tenemos claro que el éxito de nuestros proyectos se debe a las personas que forman nuestro equipo. Por eso, si cuentas con experiencia en Medical Safety / Pharmacovigilance y buscas participar en un proyecto
Quality & Regulatory Affairs Specialist | ISO 13485 | MDR Tu nueva empresa Compañía tecnológica del sector Medical Devices, especializada en el desarrollo y comercialización internacional de soluciones de software médico. La organización trabaja con productos
NESA WORLD · Donostia-San Sebastián A continuación se detalla todo lo que necesita saber sobre lo que implica esta oportunidad, así como lo que se espera de los solicitantes. En NESA WORLD diseñamos, fabricamos y comercializamos