1,192 ofertas de regulatory affairs assistant en toda España.

... tu compromiso podrás desarrollarte profesionalmente cada día. En HARTMANN tu contribución también marcará la diferencia. Únete a nuestro equipo como Como Regulatory Affairs Trainee, aprenderás a realizar comunicaciones de puesta en el mercado a la AEMPS, solicitar códigos nacionales, recabar la documentación regulatoria ...

... difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Job Details Senior Manager, Regulatory Affairs - Medical Device Summary: The Senior Manager, Regulatory Affairs - Medical Device is responsible for the execution and leadership of operational activities ...

... matters - and so do you. What's your mission? Your mission will be to provide support across all processes related to fragrance regulations managed by the Regulatory Affairs Department. Here’s what you'll be rocking every day - Control and study of different legislations, like CLP (Classification Labeling & Packaging), ...

## Promotional Regulatory Affairs Specialist, EuropeApplyremote type: Not applicablelocations: Cornella, Spaintime type: Full timeposted on: Posted Todaytime left to apply: End Date: August 22, 2026 (30+ days left to apply)job requisition id: R-2026-48303**Promotional Regulatory Affairs Specialist, Europe** *Barcelona, ...

... of our patients and customers. We foster an inclusive culture and are looking for diverse and talented individuals to join Alcon. Key responsabilities: The Regulatory Affairs Trainee will support the Regulatory Affairs team in the following activities: - Support Medical Device notification and registration activities with ...

IQVIA LLC in Madrid is seeking a Contracts Management / Reports Analyst to support Compliance Services for pharmaceutical and medical device clients. You will handle HCP contracting, grants management, and client reporting using MS Office and databases, ensuring accuracy and timely delivery.

El Regulatory Affairs Manager es responsable de garantizar que los productos farmacéuticos, biotecnológicos o dispositivos médicos cumplan con la normativa local e internacional vigente durante todo su ciclo de vida. Actúa como enlace entre la compañía y autoridades regulatorias, asegurando que la empresa mantenga el cumplimiento ...

... Imagine shaping how regulatory teams worldwide harness technology to deliver medicines faster, smarter, and with confidence. As Director, DDIT Development – Regulatory Affairs, you will be the strategic technology partner to the Regulatory Affairs organization, turning complex business priorities into a high-impact digital ...

Puig SL is seeking a Regulatory Affairs Specialist for Home Care and Chemical Compliance in Barcelona. You will ensure compliance with global chemical and cosmetic regulations, support product development, assess labeling and packaging, and manage regulatory documentation for international market access. The role requires ...

... impacto directo en el negocio? Nuestro cliente, empresa del sector cosmético en proceso de profesionalización y crecimiento, precisa incorporar un/a: TÉCNICO/A REGULATORY AFFAIRS (cosmética) Sant Cugat (Vallés Oriental) La persona seleccionada se incorporará al Departamento Técnico y asumirá de forma autónoma la gestión de los ...

Manpower ofrece una oportunidad para un Ingeniero Técnico (Calidad y Regulatory Affairs) en un entorno de ingeniería e innovación tecnológica. Se busca formar parte de un equipo que trabaje con estándares de calidad y normativas internacionales. El rol implica aprender, asumir responsabilidades y adquirir una visión global ...

Hologic, Inc. is seeking a Regulatory Affairs Specialist to join our EMEA team, taking ownership of regulatory activities across Southern Europe. You will liaise with Competent Authorities, review clinical and regulatory documentation, and ensure ongoing compliance across Greece, Spain, Portugal, Italy and Malta. Ideal ...

Data Engineer – Regulatory Affairs & Quality Medicine - Date Opened 10/22/2026 - Country Spain - Job Posting ID ZR_4493_JOB What is the mission about? . Job Description At NextLink, we are looking for an experienced Senior Data Engineer to join our consulting team and collaborate with one of our leading clients in the pharmaceutical ...

... space where Creators Of All Kinds are empowered to thrive, innovate and express who they https://jobeax.com/link/tBL6UM2EyZpq8dul OpportunityReporting to the Regulatory Affairs Manager and as part of the Safety and Regulatory Affairs Department, the role holder will be responsible for ensuring compliance with applicable chemical ...

Puig SL is seeking a Regulatory Affairs specialist to ensure compliance for the Home Care portfolio. You will support product development, assess ingredient compliance, and handle labeling, safety data sheets, and regulatory submissions. The role requires 1–2 years in regulatory affairs, knowledge of CLP and global cosmetics ...

... Creativity: an open-minded space where Creators Of All Kinds are empowered to thrive, innovate and express who they are. The Opportunity Reporting to the Regulatory Affairs Manager and as part of the Safety and Regulatory Affairs Department, the role holder will be responsible for ensuring compliance with applicable chemical ...

Senior Specialist Regulatory Affairs Raw Materials Barcelona, Spain (hybrid) Join our Raw Materials Regulatory Affairs Team, where we leverage technology and regulatory expertise to transform complex regulatory information into meaningful, actionable data. In this key role, you will contribute to global regulatory compliance ...

NextLink Group is seeking an experienced Senior Data Engineer to join our consulting team, focusing on Regulatory Affairs & Quality Medicine data domains for a leading pharmaceutical client. You will design and deploy cloud-based data pipelines in AWS, Snowflake, and SnapLogic, ensuring data quality, governance, and effective ...

... autorizaciones, liderando proyectos de desarrollo y fabricación para terceros, y coordinando presentaciones ante autoridades sanitarias. Se valora experiencia en Regulatory Affairs, dominio del eCTD Module 3 y un nivel de inglés C1. Se ofrece contrato estable, incorporación inmediata y un entorno dinámico en Madrid. [{"name": ...

... health, epidemiology, regulatory affairs, or a related field, or equivalent experience required. 4+ years of experience in Analytical/ Cell & Gene Therapy Regulatory Affairs. Mandatory technical experience in ATMP / Gene therapy; Analytical; US and EU CMC regulatory Certification in pharmacovigilance, drug safety preferred. ...