Regulatory Affairs

hace 2 semanas


Tratamiento De Aguas Goloso El, España GSK A tiempo completo

**Site Name**: GSK Tres Cantos, Madrid

**Posted Date**: Feb 19 2024

**Regulatory Affairs & Pack Management Trainee**:
**Plan de formación propuesto**:
Aquellos jóvenes Farmacéuticos que busquen crecer en un entorno global e internacional y quieran desarrollar sus competencias encontrarán en estas prácticas una oportunidad única.

**Objetivos de formación**:

- Conocer las actividades del departamento de registros y cómo llevarlas a cabo.
- Aprender el proceso de preparación y presentación de expedientes de registro de acuerdo con los diferentes procedimientos de registro.
- Aprender las implicaciones de la valoración de las fortalezas y debilidades del medicamento en desarrollo y aprender a prever posibles oportunidades y amenazas en el perfil del producto esperado.
- Conocer el proceso de revisión de materiales de acondicionamiento para conformar que cumplen con los textos autorizados.
- Aprender y colaborar en la preparación y gestión de variaciones y revalidaciones para asegurar el correcto mantenimiento del medicamento.
- Aprender y actualizar las BBDD del departamento con la información requerida.

**¿Qué perfil busca la empresa?**:

- ** Titulado universitario de **Grado en Biología, Grado en Química, Grado en Biotecnología, Grado en Farmacia o similares.
- ** Competencias en Idiomas**: nível B2 de Inglés.
- _ Capacidad de trabajo en equipo_
- _ Persona dinámica_
- _ Relaciones interpersonales_
- _ Con responsabilidad_
- _ Persona Organizada_

**¿Qué ofrece la empresa?**:

- 8h. diarias en Jornada completa
- Telepráctica semi-presencial
- Bolsa de ayuda de **800,00€** brutos mensuales
- Comedor gratuito en las instalaciones
- 25 días de vacaciones
- La beca incluye matrícula en Programa CITIUS de Iniciación profesional en la Empresa (Universidad Autónoma de Madrid)

Fecha límite: 03/03/2024

**Why Us?**

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

**Important notice to Employment businesses/ Agencies**

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.


  • Regulatory Affairs

    hace 6 días


    Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    Site Name: GSK Tres Cantos, MadridPosted Date: Apr 5 2024Regulatory Affairs & Pack Management Trainee:Plan de formación propuesto:Aquellos jóvenes Farmacéuticos que busquen crecer en un entorno global e internacional y quieran desarrollar sus competencias encontrarán en estas prácticas una oportunidad única.Objetivos de formación: Conocer las...

  • Regulatory Affairs

    hace 6 días


    Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    Site Name: GSK Tres Cantos, MadridPosted Date: Feb Regulatory Affairs & Pack Management Trainee:Plan de formación propuesto:Aquellos jóvenes Farmacéuticos que busquen crecer en un entorno global e internacional y quieran desarrollar sus competencias encontrarán en estas prácticas una oportunidad única.Objetivos de formación: Conocer las actividades...

  • Regulatory Affairs

    hace 4 semanas


    Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    **Site Name**: GSK Tres Cantos, Madrid **Posted Date**: Apr 5 2024 **Regulatory Affairs & Pack Management Trainee**: **Plan de formación propuesto**: Aquellos jóvenes Farmacéuticos que busquen crecer en un entorno global e internacional y quieran desarrollar sus competencias encontrarán en estas prácticas una oportunidad única. **Objetivos de...


  • Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    **Site Name**: Belgium-Wavre, GSK Tres Cantos, Madrid, Italy - Siena, UK - London - Brentford **Posted Date**: May 10 2023 **Director/Senior Director Global Medical Affairs Lead - Scientific Affairs & Public Health, Global Health Access**: Are you motivated by GSK’s Global Health ambition to reduce health inequalities by changing the trajectory of high...


  • Esplugues de Llobregat, España HIGH TECHNOLOGY PRODUCTS A tiempo completo

    Are you looking for experience within a Regulatory department? This is your opportunity, Sinclair are currently recruiting for a Regulatory Affairs Engineer at their Barcelona office for the Energy Devices division. The role Working within the Regulatory Affairs Team, the Junior Regulatory Affairs Specialist assures regulatory requirements are met for new...


  • Esplugues de Llobregat, Barcelona, España HIGH TECHNOLOGY PRODUCTS A tiempo completo

    Are you looking for experience within a Regulatory department? This is your opportunity, Sinclair are currently recruiting for a Regulatory Affairs Engineer at their Barcelona office for the Energy Devices division.The roleWorking within the Regulatory Affairs Team, the Junior Regulatory Affairs Specialist assures regulatory requirements are met for new...


  • Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    **Site Name**: GSK Tres Cantos, Madrid **Posted Date**: Feb 7 2024 **Therapeutic Area Director, Therapeutic Area Medical Affairs Lead (Vaccines)**: As a Director you will play a key role and will be a member of the GSK Pharma Research & Development Unit. The role reports directly into the VP Medical Director, Spain. **_ Job purpose:_** Responsible for...


  • Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    **Site Name**: GSK Tres Cantos, Madrid **Posted Date**: Jul 31 2023 **Therapeutic Area Director, Therapeutic Area Medical Affairs Lead**: As a Director you will play a key role and will be a member of the GSK Pharma Research & Development Unit. The role reports directly into the VP Medical Director, Spain. **_ Job purpose:_** Responsible for all medical...


  • l'Hospitalet de Llobregat, España Impress A tiempo completo

    Description We are **Impress**. We believe everyone deserves a smile they’ll love. We are the **largest chain of ortho clinics with fully digital processes in Europe**. We have revolutionised the invisible orthodontic sector with the best team of professionals specialised in making people smile and using the latest technology for the diagnosis,...

  • Consultant RA QA

    hace 1 mes


    El Prat de Llobregat, 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- regulatory submissions, clinical trials,...

  • Consultant RA QA

    hace 3 semanas


    El Prat de Llobregat, 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- regulatory submissions, clinical trials,...


  • Jerez de la Frontera, España Cosmewax A tiempo completo

    Descripción Buscamos un Técnico en Regulatory Affairs para nuestra sede de Jerez o Valencia. Las funciones que realizará son: - Verificar y revisar formulaciones, textos y medidas de etiquetado. - Preparar y tramitar registros de los productos finales. - Gestión de studios dermatologicos. Requisitos mínimos - Curso Experto en la Evaluación de la...


  • Distrito de Sant Martí, Barcelona, España International Staffing Consultants, Inc. A tiempo completo

    Corporate Head of Regulatory AffairsLocation: Barcelona or remote but open to commute.Job PurposeEnsure that the worldwide regulatory strategies are clearly supported and implemented in the product development, commercialization and life cycle management of the medicinal products.Major AccountabilitiesDevelopment of international regulatory strategies and...


  • Sant Feliu de Llobregat, España Centrient Pharmaceuticals Netherlands A tiempo completo

    Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms. We stand proudly at the centre of modern healthcare, as a maker of essential and life-saving medicines. With our...


  • Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    Site Name: GSK Tres Cantos, MadridPosted Date: Apr Medical Excellence Lead - ViiV HealthcareAre you interested in a Medical Affairs role that builds on your expertise in operational medical excellence, your innovative drive and your willingness and understanding of cross-functional cooperation to accelerate medical affairs engagement and excellence? If so,...


  • El Prat de Llobregat, Barcelona, España Clarivate A tiempo completo

    We are looking for a Regulatory Solutions Consultant to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA),...


  • Tratamiento De Aguas (Goloso, El), España GSK A tiempo completo

    **Site Name**: GSK Tres Cantos, Madrid, Italy - Siena, UK - Hertfordshire - Stevenage, UK - London - Brentford **Posted Date**: Jun 12 2023 Our commitment to Global Health (GH) is an important priority for GSK. The purpose of Global Health is to unite science, talent and technology to get ahead of disease together by changing the trajectory of high burden...


  • Alcalá de Henares, Madrid, España Synerlab Group A tiempo completo

    Actividades destacadas a realizar:Medical Affairs:Colaboración en todas las actividades relacionadas con las partes clínicas y preclínicas del dossier de registro de medicamentos para productos actuales y potenciales, para registro y para contestar cartas de deficiencias y variaciones regulatorias en distintos territorios. También relacionadas con food...


  • El Prat de Llobregat, España Clarivate A tiempo completo

    We are looking for a Regulatory Solutions Consultant to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA),...


  • El Prat de Llobregat, España Clarivate A tiempo completo

    We are looking for a Regulatory Solutions Consultant to join our Clinical and Regulatory Team. This is an amazing opportunity to work on regulatory consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA),...