REGULATORY AFFAIRS SPECIALIST
hace 2 semanas
Descripción del trabajo Responsibilities Support for new projects in collaboration with R&D, Marketing and Project Management Review of possible claims and communication opportunities for new projects or products already in the market Establish synergies between the different local regulatories with a global approach for the development of any new project. Ensure regulatory compliance of all the products (ingredients permitted, allowed quantities, etc...) in local and global formulations. Control and adaptation to new regulations. Preparation of packaging texts, review of proposal and approval of final artworks. Coordinate between the different local regulatories for the multilingual packaging project. Supervision and/or preparation PIF, TD, eCTD dossiers. Life cycle maintenance of these dossiers. Registration and notifications tasks of different products (food supplements, cosmetics, medical devices or OTCs) prior to its commercialization. Request of different national codes required for commercialization. Verification of the communication of marketing materials, websites, etc... Direct contact with Regulatory bodies and consultants. Direct contact with RoW partners to provide all the information and documents necessary for registration of products abroad. Post‑market surveillance activities for medical devices. Coordinate with PV department for OTCs and medical devices. Management of information (databases, SOPs…) according applicable ISO requirements (22000, 14001, 13485…) Sector: Industria Farmacéutica Función: Salud / Medicina Crear una alerta de empleo para esta búsqueda #J-18808-Ljbffr
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NAT Regulatory Affairs Specialist
hace 2 días
Sant Cugat del Vallès, España Grifols, S.A A tiempo completoA global healthcare company is seeking a Nucleic Acid Testing (NAT) Regulatory Affairs Specialist to join their Diagnostic Regulatory Affairs department. The candidate will prepare technical documentation, manage product registrations, and ensure compliance with regulations. Applicants should possess a Bachelor's in Health Sciences, experience in Regulatory...
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NAT Regulatory Affairs Specialist
hace 2 semanas
Sant Cugat, España Grifols, S.A A tiempo completoA global healthcare company is seeking a Nucleic Acid Testing (NAT) Regulatory Affairs Specialist to join their Diagnostic Regulatory Affairs department. The candidate will prepare technical documentation, manage product registrations, and ensure compliance with regulations. Applicants should possess a Bachelor's in Health Sciences, experience in Regulatory...
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sant cugat del vallès, España Grifols A tiempo completoA global healthcare company is looking for a Regulatory Affairs Specialist in Sant Cugat del Vallès. The role includes managing regulatory submissions, ensuring compliance with international regulations, and working in a hybrid model. Candidates should have a Bachelor's degree in a relevant field and 2-5 years of experience in regulatory documentation....
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Sant Cugat del Vallès, España Grifols A tiempo completoA global healthcare company is looking for a Regulatory Affairs Specialist in Sant Cugat del Vallès. The role includes managing regulatory submissions, ensuring compliance with international regulations, and working in a hybrid model. Candidates should have a Bachelor's degree in a relevant field and 2-5 years of experience in regulatory documentation....
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Regulatory Affairs Specialist
hace 4 días
sant cugat del vallès, España Grifols, S.A A tiempo completoWould 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 been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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Regulatory Affairs Specialist
hace 4 días
sant cugat del vallès, España Grifols A tiempo completoWould 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 been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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sant cugat del vallès, España Grifols A tiempo completoA global healthcare company is seeking a Nucleic Acid Testing Regulatory Affairs Specialist in Sant Cugat del Vallès. The role involves preparing regulatory documents, coordinating submissions, and defining regulatory requirements. Candidates should have a Bachelor's in Health Sciences, experience in pharmaceutical RRAA, and advanced skills in Spanish and...
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Regulatory Affairs Specialist
hace 2 semanas
Sant Cugat del Vallès, España Grifols A tiempo completoWould 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 been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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Regulatory Affairs Specialist – French Native
hace 3 días
sant cugat sesgarrigues, España Uriach A tiempo completoA leading pharmaceutical company in Spain is seeking an Entry-Level Regulatory Affairs Specialist who is a native French speaker. In this role, you will support new projects, ensure compliance with regulations, and manage communication with regulatory bodies. Ideal candidates should be passionate about regulatory affairs and willing to collaborate with...
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Sant Cugat, España Grifols, S.A A tiempo completoA global healthcare company in Sant Cugat del Vallès seeks a Regulatory Affairs Specialist Lab Automation to enhance regulatory compliance. This hybrid position requires a Bachelor's degree in a Life Sciences field and 2-5 years of regulatory experience, specifically with IVDR and FDA regulations. The role involves maintaining interfaces with regulatory...
