Trabajo de Regulatory Affairs Associate en Aragón

Hace 1 día Sé de los primeros 25 solicitantes Enviar mensaje directo al anunciante de SOMVITAL En el laboratorio no solo se miden parámetros: se cuida la esencia de lo que ofrecemos. Cada certificado, cada validación, cada ficha técnica representa mucho más que un trámite: es la garantía de que nuestros productos cumplen con los más altos estándares y llegan al mercado con rigor y...

Somos un grupo internacional innovador, con amplia experiencia en la comercialización de productos farmacéuticos en el ámbito geográfico de Centroamérica y el Caribe.Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado.Objetivo principal del puesto:Gestionar los registros sanitarios de los diferentes productos...

Overview Job Description Summary As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. Job Description Main responsibilities include: - GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customers -...

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France (Eybens) or Spain (San Agustin Del Guadalix). You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, and internal stakeholders. You will contribute to strategic regulatory analysis,...

A global healthcare company located in Spain is seeking a QA Officer to ensure quality oversight for GMP activities. Responsibilities include supervising hygiene conditions, managing quality documentation, and supporting audits. The ideal candidate will have a scientific degree in Pharmacy, Chemistry, or Biology, along with at least 1 year of experience in a Quality department. Proficiency in...

About the company OMODA Motors, part of the Chery Group, is an international automotive brand expanding in Europe. Our European headquarters is in Barcelona, leading the brand’s development across the region.Work arrangement This position is based fully on-site at our Barcelona office.Why join us? • Join one of the fastest-growing global automotive brands leading innovation in Europe.• Shape...

Medical Science Liaison – Spain Role: Full-time, permanent Location: Barcelona, SpainThe Role: As a result of the continuous growth of our company and upcoming launches of new original products, we are now looking to hire our first Medical Science Liaison within Spain.We’re seeking a driven and organised individual to act as a scientific and medical field-based expert to external and internal...

Overview As we strive to be Earth's Safest Place to Work, we are expanding the Japan Workplace Health and Safety organization and are seeking a Director, Safety Operations, Japan. This mission-driven role will directly impact thousands of employees by ensuring safe home-to-work and back daily, while leading the implementation of a comprehensive safety strategy to promote safe and efficient...

Research Nurse – Decentralized & Hybrid Clinical Trials (Barcelona) Barcelona, Spain Clinical Research | Patient‑Centric Care | Remote & On‑Site Operations Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista. Lea la descripción completa del puesto a continuación.About the Role A growing clinical research organization in Barcelona is...

Overview The QA Officer guarantees the quality oversight over the entire working time of the facility for all the GMP activities on going. About The Role - Supervise the general conditions of hygiene of the premises subject to its management - Contribute in assuring the validation/qualification status of the production site, equipment, training of personnel and management of quality...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

Una empresa enfocada en la calidad en salud animal busca un profesional para gestionar sus Sistemas de Gestión de Calidad y participar en proyectos de I+D. Se requiere formación universitaria en áreas afines, experiencia en funciones similares, y conocimientos técnicos en gestión de calidad y análisis microbiológicos. La empresa ofrece formación continua y oportunidades de desarrollo. Envía tu CV...

Overview As we strive to be Earth's Safest Place to Work, we are expanding the Japan Workplace Health and Safety organization and are seeking a Director, Safety Operations, Japan. This mission-driven role will directly impact thousands of employees by ensuring safe home-to-work and back daily, while leading the implementation of a comprehensive safety strategy to promote safe and efficient...

A prominent medical technology company in San Agustín del Guadalix is seeking a Regulatory Affairs Trainee to support the EMEA team with GTM activities in Spain and Portugal. Responsibilities include handling product notifications and assisting with CE mark activities and international registrations. Candidates must have a university degree in Life or Engineering Science or equivalent, and an...

Una empresa enfocada en la calidad en salud animal busca un profesional para gestionar sus Sistemas de Gestión de Calidad y participar en proyectos de I+D. Se requiere formación universitaria en áreas afines, experiencia en funciones similares, y conocimientos técnicos en gestión de calidad y análisis microbiológicos. La empresa ofrece formación continua y oportunidades de desarrollo. Envía tu CV...

Summary The QA Officer guarantees the quality oversight over the entire working time of the facility for all the GMP activities on going. About The Role Major accountabilities: - Supervise the general conditions of hygiene of the premises subject to its management - Contribute in assuring the validation/qualification status of the production site, equipment, training of personnel and...

Overview As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. Main responsibilities - GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customers - BD, SA manufacturer: CE mark activity,...

A leading global medical technology company is seeking a Regulatory Affairs Trainee in San Agustín del Guadalix, Spain. The role involves supporting GTM activities and coordinating with national authorities, along with managing product notifications and audits. Candidates should possess a university degree related to Life or Engineering Science and hold an internship agreement with their...