Regulatory Affairs Consultant

hace 2 meses


Barcelona, España Ramboll Group AS A tiempo completo

We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment.Are you our new Regulatory Affairs Consultant?Click theI'm Interested -button to send your application.Inviting bright mindsDo you want to push the boundaries of your profession and develop your excellence in an open, collaborative and empowering culture?
We work to create a sustainable future and our inspiring projects and innovative solutions aim to set the standard among our peers.
You will join a global company that has been growing successfully since its founding in 1945.
Together, we lead and leave a positive impact on societies, companies and people around the world.You will join our international Health Sciences service line:As our new expert in biocides, you will be part of an established international team of Product Safety and Stewardship specialists, delivering key knowledge to a range of Ramboll projects.
Our regulatory scientists characterise and effectively communicate the potential risks from chemicals and product uses and identify options for safe, state-of-the-science stewardship.Our successful global track record includes evaluations and stewardship for chemical producers, biocides, food and food packaging, building materials, toys, cosmetics, aerospace manufacturing, medical device and electronic device manufacturing, and pesticides.Your key tasks and responsibilities will be:Providing technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in SpainParticipating on projects relating to REACH, BPR etc.Collaborating with colleagues so that the product authorization and active substance approval files advance in a timely and effective mannerWorking with the team to carry out the dossiers according to ECHA standards.Collaborating with the Senior Consultants in Health SciencesParticipating in activities prior to projects (such as offers etc).Experience in any of the following would be advantageous:Providing authorisation strategies and regulatory advice for clients (including development of testing programmes for biocides and industrial chemicals)Compiling approval/authorisation dossiers according to the EU and GB Biocidal Products RegulationPerforming hazard, exposure and risk assessment, and/or efficacy assessments, in your field of expertiseCoordinating collaborative and timely preparation of application dossiers together with our subject matter expertsDeveloping and maintaining a comprehensive understanding of the current and future regulatory landscape, attending conferences to keep up to date with developments in the appropriate laws and guidanceParticipating in business development activities by providing industry expertise when needed during visits to clients, through discussion and responses to new project briefs and administrationYour starting point for constant growthFrom the moment you join Ramboll, we will support your personal and professional development so that you grow with the company.
For this role, we believe your starting point is:Strong academic background with, as a minimum, a relevant science-based degree (e.G.
biology, chemistry, biochemistry, pharmacology)Minimum of 2 years' experience working in regulatory affairs or product safety, ideally in the chemicals industryKnowledge of European regulations (REACH, BPR and other RoHS directives etc).Experience of carrying out Risk Assessments (Environmental, biological, human etc).Experience of using ECHA IT tools and portals: REACH IT, IUCLID, SPS Editor, SCIPFluency in written and verbal English is essential; knowledge of French, Portuguese or other language highly desirablePersonal skills that will help you succeed in this role:Pro-activity, eager to learn and grow in an international environment, customer focus, communication skills, attention to detail.Welcome to our Environment & Health divisionRamboll develops innovative, scientifically sound solutions that help increase livability by reducing pollution and restoring natural environments as well as incorporating sustainability principles across all steps of the projects.
One of the world's leading environmental and health consultancies, our bright minds are trusted by clients to manage their most challenging environmental, health and social issues.Ramboll in IberiaRamboll has undertaken projects in Spain and Portugal since the 1990's and operates offices in Barcelona and Madrid since 2006.
Our +70 professionals apply their broad international experience to deliver innovative solutions aimed at making our societies more resilient and more sustainable.
We support national and international clients and our work involves daily collaboration with a broad team of experts located in our Business Units across the globe.
We love seeing our talents develop and succeed and you will have opportunities to work on challenging and inspiring projects within an environment that is friendly, flexible, open and supportive.How to applyApply online.
Attach your CV, cover letter and relevant documents showcasing why you are the right fit for the role, and when you are available to start.
We look forward to receiving your application.Additional InformationAll your information will be kept confidential according to EEO guidelines.#J-18808-Ljbffr



  • Barcelona, España Lhh A tiempo completo

    Desde la división de LifeSciences de LHH Recruitment Solutions estamos seleccionando el perfil de Regulatory Affairs Consultant para formar parte de importante Consultoría Farmacéutica.TAREASPreparar la documentación requerida para obtener el marcado CE, FDA o registros de otros países según la legislación vigente.Gestión de diversos proyectos de...


  • Barcelona, España LHH A tiempo completo

    Desde la división de LifeSciences de LHH Recruitment Solutions estamos seleccionando el perfil de Regulatory Affairs Consultant para formar parte de importante Consultoría Farmacéutica. TAREAS - Preparar la documentación requerida para obtener el marcado CE, FDA o registros de otros países según la legislación vigente. - Gestión de diversos...


  • Barcelona, España Lhh A tiempo completo

    Desde la división de LifeSciences de LHH Recruitment Solutions estamos seleccionando el perfil de Regulatory Affairs Consultant para formar parte de importante Consultoría Farmacéutica.TAREAS- Preparar la documentación requerida para obtener el marcado CE, FDA o registros de otros países según la legislación vigente.- Gestión de diversos proyectos de...


  • Barcelona, España Alira Health A tiempo completo

    Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...

  • Consultant Ra QA

    hace 6 meses


    Barcelona, España Clarivate A tiempo completo

    Consultant RA QA - ( Regulatory Affairs / Quality Assurance ) - Barcelona ( Hybrid ) We are looking for a RAQA Consultant ( Regulatory Affairs / Quality Assurance ) to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory and quality consulting projects. We have a great skill set in data monitoring, content writing and...


  • Barcelona, España Ramboll Group AS A tiempo completo

    .We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment. Are you our new Regulatory Affairs Consultant? Click the I'm...

  • Regulatory Affairs

    hace 6 meses


    Barcelona, 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...

  • Regulatory Affairs

    hace 6 meses


    Barcelona, 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 RegistrosTus funciones serán las siguientes:- Elaborar, mantener y actualizar los dossiers de los medicamentos y los expedientes técnicos de los productos de la empresa.- Colaborar...


  • Barcelona, España Ramboll Group AS A tiempo completo

    .We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment.Are you our new Regulatory Affairs Consultant? Click the I'm...


  • Barcelona, España buscojobs España A tiempo completo

    Regulatory Affairs AssociateBarcelona, CataloniaGalderma - 28.11.2024With 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 approach to dermatological care.Regulatory Affairs AssociateBarcelona, CataloniaGlobal...


  • Barcelona, España buscojobs España A tiempo completo

    Regulatory Affairs AssociateBarcelona, CataloniaGalderma - 28.11.2024With 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 approach to dermatological care.Regulatory Affairs AssociateBarcelona, CataloniaGlobal...


  • Barcelona, Barcelona, España Werfen A tiempo completo

    The Regulatory Affairs department at Werfen is seeking a highly skilled Quality and Regulatory Affairs specialist to join our team in Barcelona, Spain.As a Quality and Regulatory Affairs specialist, you will be responsible for supporting the execution of pre and post-market regulatory affairs departmental functions. This includes assisting in the preparation...

  • Consultant Ra QA

    hace 6 meses


    Barcelona, España Clarivate A tiempo completo

    We are looking for a **RAQA Consultant** **( Regulatory Affairs / Quality Assurance ) **to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory and quality consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains **About You - experience, education, skills,...


  • Barcelona, 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,...


  • Barcelona, Barcelona, España FARMAPROJECTS SAU A tiempo completo

    Farmaprojects SAU is a B2B Pharmaceutical Laboratory company offering a broad portfolio of generic pharmaceutical products and value-added medicines. We are looking for a Regulatory Affairs Senior Specialist to join our Regulatory Affairs Department.Key responsibilities include:Developing assessments and strategic regulatory plans for strategic product...


  • Barcelona, 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...


  • Barcelona, España Hartmann A tiempo completo

    Únete 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 técnica y su...


  • Barcelona, España HARTMANN A tiempo completo

    Únete 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...


  • Barcelona, España Ramboll Group AS A tiempo completo

    We invite you to bring your knowledge of European regulations governing product safety and stewardship into play as you support organisations around the world bring to the market products in a range of uses that meet relevant requirements and are safe for human health and the environment.Are you our new Regulatory Affairs Consultant? Click the I'm...

  • Regulatory Affairs

    hace 6 meses


    Barcelona, España Hays A tiempo completo

    **Tu nueva empresa** Nuestro cliente es una empresa en pleno crecimiento que se dedica a la investigación de ingredientes patentados para su aplicación en diferentes sectores: alimentación, salud y nutrición. **Tu nuevo puesto** Estamos buscando perfiles como Regulatory Affairs Manager & Regulatory Affairs Technician, cuyo objetivo será el de...