Trabajo de Regulatory en Zaragoza

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...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload. The Regulatory Submissions Specialist...

Buscamos un/a Regulatory Affairs para una empresa industrial de la zona de Sant Cugat. Si tienes experiencia en regulación de biocidas, cosméticos y dispositivos médicos, y buscas un nuevo reto en un entorno dinámico, ¡Queremos conocerte! Responsabilidades: Seguimiento de cambios normativos y evaluación de impacto en productos y procesos. Gestión de expedientes de registro y coordinación de...

A growing healthcare consultancy firm is seeking Regulatory professionals to join their international team in Spain. This role includes providing expert guidance on various biological products and managing complex regulatory strategies. The ideal candidate will have a solid understanding of CMC requirements, excellent English skills, and be proficient in a local language. The position involves...

A leading consulting firm in Spain seeks a detail-oriented individual to manage registration processes and product data. Responsibilities include maintaining regulatory communications, supporting product updates, and ensuring data quality compliance. This role requires strong data management skills but no prior experience is necessary. It is ideal for someone proficient in Microsoft Office and...

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...

Health in Code es una empresa líder en diagnóstico genético, comprometida con mejorar la calidad de vida de las personas a través de la medicina personalizada y la toma de decisiones clínicas basadas en datos genómicos. ¿Te interesa el ámbito de Regulatory Affairs y quieres formarte en el ciclo de vida del producto sanitario de diagnóstico genético dentro de un entorno altamente...

Mediktor is looking for a QA/RA specialist! Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada.If you are passionate about applying the regulation to cutting edge technology and you would like to discover the Software Medical Device regulation, we are looking for you! The Team:As a member of the Quality...

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...

Position Overview ¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring...

Asphalion is growing and we are looking for a Regulatory Affairs Senior Officer to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to work in an international environment and who wants to grow with us! Main responsibilities: Global CMC writing/management of product specific dossiers (Mod. 2/Mod. 3), with special focus on biologics...

Experteer OverviewYou will drive global regulatory labeling work to ensure accurate patient information and compliance. You collaborate with cross-functional teams to prepare and update SmPC, PIL, and labelling for EU and non-EU markets, shaping product information for diverse stakeholders. You navigate labeling governance processes, support product lifecycle management, and provide regulatory...

A global pharmaceutical company in Zaragoza is seeking a Compliance Specialist to maintain and develop quality systems strategy and ensure compliance with regulatory and GMP requirements. The ideal candidate will have a Bachelor's Degree in Pharmacy or an MSc in Pharmaceutical Industry, and at least 2 years of experience in GxP operations, including 1 year in Quality Assurance. Excellent...

Please note this position can be located in our offices in Barcelona with 2 days on site.Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación.G&L Scientific is a specialist provider to the healthcare industry for all types of Regulatory Affairs and Quality Assurance consultancy work – and we are...

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 BD, SA...

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, international...

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...

Descripción del trabajo Position Overview The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and global regulatory...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved in and ensures that the outputs of their activities meet the quality...

Job Description Summary Responsible for supporting and executing regulatory activities across multiple projects and UCC and Surgery product lines to ensure compliance with industry standards and regulatory requirements. This role involves reviewing and approving advertising and promotional materials, managing regulatory and product related documentation, providing local regulatory support, and...