Senior Regulatory Affairs Specialist
hace 2 meses
Would 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 develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.We are looking for a Senior Regulatory Affairs Specialist to join Biopharma Regulatory department.What your responsibilities will bePrepare, review, and manage complex submissions and follow up of product registrations or any other regulatory activity, ensuring timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.Communicate with affiliates, outside companies and Health Authorities.Represent the regulatory function on project teams as related to worldwide product registrations.Adapt licenses to current regulations.Maintain tracking of product registrations.Support other Departments, Affiliates and Third Parties in any required regulatory information.Create regulatory affairs policies and procedures.Who you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Bachelor's Degree in Life Sciences field is preferred.Minimum 2 years of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of education and experience.Experience with applicable worldwide regulatory product registrations laws and regulations.Experience of eCTD/CTD submissions, and dossier lifecycle management.Advanced level of English.User of Microsoft Office tools.You are meticulous and detail-oriented.You have excellent communication and teamwork skills, as well as initiative and results orientation.What we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to applyWe look forward to receiving your applicationGrifols is an equal opportunity employer.Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.Benefits packageContract of Employment: Temporary positionFlexibility for U Program: Hybrid
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Senior Regulatory Affairs Specialist
hace 2 meses
España Grifols A tiempo completoSenior Regulatory Affairs Specialist Barcelona Would 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...
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Senior Regulatory Affairs
hace 3 semanas
España Antal International A tiempo completoDesde el departamento de Pharma de Antal International nos encontramos en búsqueda de un Senior Regulatory Affairs para trabajar en una importane multinacional Dermocosmética para la parte de regulación de medicamentos ubicada en Barcelona. **Requisitos**: - Formación Universitaria en Ciencias de la Salud - Más de 4 años con posiciones de Regulatory...
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Senior Regulatory Affairs Specialist
hace 1 semana
España Jordan martorell s.l. A tiempo completo¿Tienes experiencia como Técnico/a de Registros dentro del sector farmacéutico? ¿Tienes disponibilidad para desplazarte para la zona de Martorelles?Desde ManpowerGroup Talent Solutions estamos buscando un/a Técnico/a de Registros (R&D Regulatory Affairs Specialist). Dicha posición estará asignada al equipo de R&D para una empresa multinacional del...
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Senior Regulatory Affairs Specialist
hace 3 días
España ManpowerGroup A tiempo completo¿Tienes experiencia como Técnico/a de Registros dentro del sector farmacéutico? ¿Tienes disponibilidad para desplazarte para la zona de Martorelles?Desde ManpowerGroup Talent Solutions estamos buscando un/a Técnico/a de Registros (R&D Regulatory Affairs Specialist). Dicha posición, estará asignada al equipo de R&D, para empresa multinacional del...
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Regulatory Affairs Specialist- EBD
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Regulatory Affairs Specialist
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España Innovaderm Research A tiempo completoDue to ongoing global expansion, Innovaderm is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and/or part II following EU CTR and other applications created within or outside of the company to ensure documentation comply with applicable regulations and guidelines and...
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[I838] Regulatory Affairs
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Regulatory Affairs Senior Specialist EMEA M/F
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Regulatory Affairs Senior Specialist EMEA M/F
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España PQE Group A tiempo completoAre you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.Due to our constant growth, we are looking for a Regulatory Affairs Specialist to...
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Regulatory Affairs Associate
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Regulatory Affairs
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España Hays A tiempo completo**Tu nueva empresa** Reconocido Laboratorio Farmacéutico ubicado a escasos KM de Barcelona. **Tu nuevo puesto** Precisamos incorporar un perfil de Regulatory Affairs - Técnico de Registros Tus funciones serán las siguientes: - Elaborar, mantener y actualizar los dossiers de los medicamentos y los expedientes técnicos de los productos de la...
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Associate Director, Regulatory Affairs
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[Ib-679] | Quality Assurance
hace 3 días
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Regulatory Affairs Specialist
hace 4 semanas
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hace 2 meses
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España Page Personnel España A tiempo completoTécnico/a para la preparación de la documentación regulatoria de los productos desarrollados por la empresa, complementos alimenticios, productos sanitarios clase IIa, productos sanitarios in vitro y cosméticos. Formación en Ciencias de la Salud|Prácticas en RA y/o Máster en Registros - Formación en Ciencias de la Salud: Farmacia, biología,...
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Senior Regulatory Affairs Engineer
hace 2 meses
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