Senior Regulatory Affairs Specialist

hace 2 meses


España Grifols A tiempo completo

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
#J-18808-Ljbffr



  • España Grifols A tiempo completo

    Senior 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...

  • Senior Regulatory Affairs

    hace 3 semanas


    España Antal International A tiempo completo

    Desde 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...


  • 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...


  • 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...


  • España The Zonal Group A tiempo completo

    Job Details: Regulatory Affairs Specialist- EBDFull details of the job. Vacancy Name Vacancy Name Regulatory Affairs Specialist- EBD Vacancy No Vacancy No VN309 Employment Type Employment Type Full-Time Location About the JobSinclair is looking for a Regulatory Affairs Specialist to manage the global product...


  • España Innovaderm Research A tiempo completo

    Due 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...


  • España buscojobs España A tiempo completo

    ResumenBuscamos un Regulatory Affairs Specialist cuya misión será el aseguramiento del cumplimiento regulatorio de las fragancias para su aplicación, dando soporte regulatorio tanto a nivel interno a los departamentos que lo necesiten y externo a Clientes.ResponsabilidadesEntre sus principales funciones se encuentra el análisis y actualización de datos...


  • España Jordan martorell s.l. A tiempo completo

    Regulatory Affairs Senior Specialist EMEA M/FWe are ZimVie, a publicly traded, global life sciences leader focused on restoring daily life to our patients by designing, manufacturing, and distributing a comprehensive portfolio of innovative tooth replacement and spine surgery solutions. Our company is founded on a legacy of trusted brands, products, and...


  • España ZimVie Inc. A tiempo completo

    Select how often (in days) to receive an alert:Regulatory Affairs Senior Specialist EMEA M/FJob Function: RegulatoryLocation: Cornella de Llobregat, B, ESWe are ZimVie, a publicly traded, global life sciences leader focused on restoring daily life to our patients by designing, manufacturing, and distributing a comprehensive portfolio of innovative tooth...


  • España PQE Group A tiempo completo

    Are 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...


  • España Galderma Pharma S.A A tiempo completo

    Regulatory Affairs Associate With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology...

  • Regulatory Affairs

    hace 3 semanas


    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...


  • España Cpl Healthcare A tiempo completo

    Job Title: Associate Director, Regulatory Affairs - Medical Device/Post-Market SurveillanceJob Type: Full Time, Permanent PositionLocation: Spain, Madrid – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to...


  • España buscojobs España A tiempo completo

    (IB-679) | Quality Assurance & Regulatory Affairs Specialist - Temporary PositionMadridEUR 50.000 - 70.000Quality Assurance & Regulatory Affairs Specialist - Temporary positionJob Description:At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on...


  • España HARTMANN A tiempo completo

    Únase a nuestro equipo como **Regulatory Affairs Trainee** ESP-Mataró (Barcelona) Aprovecha la nueva oportunidad que te ofrece HARTMANN en el Área de Regulatory Affairs. **Responsabilidades** En relación con las comunicaciones de puesta en el mercado a la AEMPS por cada producto sanitario que ponemos en el mercado: - Reunir la documentación...


  • España MCR International A tiempo completo

    LAR-2411-365REGULATORY AFFAIRS ASSOCIATE DIRECTORMADRIDRegulatory Affairs Associate Director Opportunity – Join a Leading Pharmaceutical Company in Madrid, Spain!At MCR International, we're thrilled to announce an exclusive opportunity for a Regulatory Affairs Associate Director with a renowned global pharmaceutical company. This strategic role, based in...


  • España Puig A tiempo completo

    The OpportunityResponsible for ensuring regulatory compliance of finished cosmetic products during all the key phases of the product development.What you'll get to doProvide regulatory alerts and constraints during marketing brief for new projects.Perform formula and raw material checks: verify global compliance regarding ingredients and...


  • España Angelini Pharma España A tiempo completo

    Dentro del Departamento de **Regulatory Affairs & QA**, la posición de** Trainee **Regulatory Affairs **está enfocada a dar soporte principalmente el área de Regulatory Affairs en el cumplimiento de los estándares de calidad de los productos comercializados de acuerdo con la normativa vigente a nível nacional y europeo y las directrices establecidas por...


  • España Page Personnel España A tiempo completo

    Técnico/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,...


  • España AbleCloset A tiempo completo

    Job Details: Senior Regulatory Affairs Engineer (Pre-Market)Full details of the job.Vacancy Name: Senior Regulatory Affairs Engineer (Pre-Market)Vacancy No: VN179Employment Type: Full-TimeLocation: Esplugues del Llobregat (Barcelona)The RoleSinclair is currently looking for a Pre-Market Regulatory Affairs Engineer at its offices located in Esplugues del...