Trabajo Regulatory - Cerdanyola Del Vallès

The QA Scientist will be assigned the following responsibilities: Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released. Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA ...

We are hiring a Qualified Person (QP) for our Quality Assurance Department The Qualified Person (QP) will be assigned the following responsibilities: Review and approve the documentation involved in the analytical activity of the company: CoA, Site Master File, SOPs, product specifications. Particip...

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance Department. The QA Scientist will be assigned the following responsibilities: Review and approve the documentation involved in the analytical activity of the company: CoA, protocols, reports, SOPs, product specificatio...

Descripción de la oferta de empleoPerfil buscado (Hombre/Mujer)• Trabajar juntamente con los equipos de Medico-Marketing para diseñar un Plan de Acción Digital/Omnicanal (Channel mix) acorde a (i) las necesidades del cliente, (ii) los objetivos del producto/marca y (iii) las posibilidades que ofrece...

Reportando a Dirección Técnica, te responsabilizarás de:- Supervisión de Cumplimiento Regulatorio: Asegurar que todos los productos y procesos cumplan con las normativas locales e internacionales.- Gestión de Documentación: Coordinar la preparación y presentación de documentos regulatorios a las aut...

¿Dónde vas a trabajar? An international personal care company with an important presence in Spain in pharmacy channel and retail, needs to incorporate a Product developer (Medical Devices) for the R&D and Regulatory team. ¿Qué harás en tu nuevo puesto? An international personal care company with ...

¿Dónde vas a trabajar? Multinational mining company located in Barcelona city ¿Qué harás en tu nuevo puesto? Team Leadership: Provide leadership and direction to the audit team, fostering a collaborative and high-performance work environment. Mentor, train, and develop team members to enhance t...

¿Dónde vas a trabajar? Multinational mining company located in Barcelona city ¿Qué harás en tu nuevo puesto? Participate in planning and conducting audit engagements, including gathering documentation, performing audit tests, and analyzing data. Follow audit procedures and methodologies to asses...

¿Dónde vas a trabajar? PageGroup SSC ¿Qué harás en tu nuevo puesto? Training Program Coordination Coordinate activities for training sessions, workshops, and learning events. Schedule training sessions and manage resources required for training delivery when applicable. Allocate trainers' reso...

¿Dónde vas a trabajar? PageGroup SSC ¿Qué harás en tu nuevo puesto? Training Program Coordination Coordinate activities for training sessions, workshops, and learning events. Schedule training sessions and manage resources required for training delivery when applicable. Allocate trainers' reso...

¿Dónde vas a trabajar? PageGroup SSC ¿Qué harás en tu nuevo puesto? Training Program Coordination Coordinate activities for training sessions, workshops, and learning events. Schedule training sessions and manage resources required for training delivery when applicable. Allocate trainers' reso...

Main task Design the mechanics of the medical device, adapting the electronic circuits and components of BraiN20 device and redesign the performance and assembly Secondary tasks - Collaborate with hardware designers, testers, biomedical engineers, and firmware and hardware engineer to develop device...

- Support the development of the CMCD (Chemistry, Manufacturing, and Controls Development) strategy for certain products of the business unit, both mature and new launch, to ensure globally approvable dossiers.- Responsibility is shared across global and local markets.- Work closely with Regulatory ...

¿Dónde vas a trabajar? Compañía en crecimiento precisa incorporar un Regulatory Affairs Officer a su plantilla. ¿Qué harás en tu nuevo puesto? Recopilación y redacción de documentación CMC para los nuevos dosieres de registro. Gestión de los trámites regulatorios con las autoridades sanitarias p...

¿Dónde vas a trabajar? A Biopharmaceutical company is looking for a Medical Monitor - Oncology ¿Qué harás en tu nuevo puesto? The Medical Monitor collaborates in the overall global (US/EU) clinical development for oncology compounds, taking into consideration both medical and scientific issues. S...