Trabajo de Regulatory Affairs en Zaragoza

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...

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...

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...

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,...

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 propósito. Si...

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...

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...

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...

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...

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...

We are seeking experienced freelance Clinical Research Nurses to support an Acute Ischaemic Stroke study. This is an ad-hoc role with flexible scheduling, ideal for nurses currently working freelance or supporting multiple clients. Visits will be scheduled well in advance.Study Overview Study Duration: 20 months Visit Duration: Approximately 2 hours per visitKey ResponsibilitiesConduct patient...

In a few wordsLa experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.Position: Biotech Senior Project ManagerLocation: MadridExperience: +5 years in biotech project managementWant to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized...

Director de Compras para empresa farmacéutica con actividad en salud humana, veterinaria y CDMO debe combinar perfil técnico-regulatorio, visión estratégica y capacidad de gestión internacional. Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura. Misión del puesto: Definir y ejecutar la...

JOB OFFER: Market Access Registration Specialist Location Huesca About the Company We are a global company in the animal nutrition and feed industry, committed to innovation, quality, and strict regulatory compliance across international markets. Our Market Access team plays a key role in ensuring our products reach target markets with all required regulatory approvals. We are looking for a...

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. ¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar. This position is based fully on-site at our...

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...

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...

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...

Our team members are at the heart of everything we do. At Cencora we are united in our responsibility to create healthier futures and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Cencora...

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...