- Proactively provide strong QA leadership to the business strategy for assigned trials by ensuring considerable organization awareness (e. g. Interrelationship of departments and business priorities)
- Support implementation of the quality strategy within GCT under responsibility.
- Regularly monitor the implementation of the annual Quality Plan pertaining to the Clinical chapter and ensure that all delayed activities have a documented rational and appropriate escalation.
- Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that CTP processes are in control
- Provide robust and clear quality oversight in various areas of clinical development.
- Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
- Support continuous improvement initiatives (including Work streams)and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
- Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.
- Proactively provide strong QA leadership to the business strategy for assigned trials by ensuring considerable organization awareness (e. g. Interrelationship of departments and business priorities)
- Support implementation of the quality strategy within GCT under responsibility.
- Regularly monitor the implementation of the annual Quality Plan pertaining to the Clinical chapter and ensure that all delayed activities have a documented rational and appropriate escalation.
- Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that CTP processes are in control
- Provide robust and clear quality oversight in various areas of clinical development.
- Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
- Support continuous improvement initiatives (including Work streams)and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
- Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.
- Proactively provide strong QA leadership to the business strategy for assigned trials by ensuring considerable organization awareness (e. g. Interrelationship of departments and business priorities)
- Support implementation of the quality strategy within GCT under responsibility.
- Regularly monitor the implementation of the annual Quality Plan pertaining to the Clinical chapter and ensure that all delayed activities have a documented rational and appropriate escalation.
- Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that CTP processes are in control
- Provide robust and clear quality oversight in various areas of clinical development.
- Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
- Support continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
- Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.
- Proactively provide strong QA leadership to the business strategy for assigned trials by ensuring considerable organization awareness (e. g. Interrelationship of departments and business priorities)
- Support implementation of the quality strategy within GCT under responsibility.
- Regularly monitor the implementation of the annual Quality Plan pertaining to the Clinical chapter and ensure that all delayed activities have a documented rational and appropriate escalation.
- Ensure adequate oversight of proactive quality risk management process in the overseen areas including quality risk assessments and submission/inspection readiness activities and ensure that CTP processes are in control
- Provide robust and clear quality oversight in various areas of clinical development.
- Actively leverage audit/inspection outcomes/trends to sustain improvement in clinical trials conduct.
- Support continuous improvement initiatives (including Work streams) and ensure that areas identified as weaknesses are properly being addressed and executed for sustainability
- Be QA point of contact for the defined trials and attend the meetings and ensure quality is embedded in the decision taking processes.
- Proactively provide strong QA leadership to the business strategy for assigned trials by ensuring considerable organization awareness (e. g. Interrelationship of departments and business priorities)
- Support implementation of the quality strategy within GCT under responsibility.
- Regularly monitor the implementation of the annual Quality Plan pertaining to the Clinical chapter and ensure that all delayed activities have a docu
-
QA (Quality Assurance)
hace 5 días
Top Doctors Barcelona, EspañaEn grupo **Top Doctors** seguimos creciendo · ¿Quieres unirte a la empresa que ha revolucionado el sector de la medicina privada, así como la tecnología médica y que en los próximos años se va a consolidar como la empresa líder de eHealth en el mundo? · Grupo Top Doctors es la em ...
-
Quality Assurance Technician
hace 1 semana
Mango Barcelona, EspañaEn Mango inspiramos y unimos mediante nuestra pasión por el estilo y la cultura. Estamos en 118 países y nuestra presencia online se extiende a más de 80 países. Nuestro equipo está formado por personas de 112 nacionalidades y en un 80% por mujeres. · Buscamos un/a · QUALITY ASSU ...
-
Quality Assurance Technician
hace 3 días
Talent Search People Barcelona, España Sin especificarDesde Talent Search People, Buscamos incorporar un/a Técnico/a de Garantía de Calidad Compliance para el departamento de Garantía de Calidad de la Planta Química para una compañía farmacéutica de referencia a nível global con presencia internacional. · Tareas · **En tu día a día* ...
-
Quality Assurance Manager
hace 1 semana
NonStop Consulting Barcelona, España**Principales Funciones**: · - Asegurar la adecuación de la producción en Salas Blancas a los requisitos establecidos de Calidad. - Comprobar el cumplimiento de la normativa y regulación de Calidad en todos los aspectos de la cadena de valor - Realización de informes técnicos y a ...
-
Quality Assurance Trainee
hace 1 día
Ferrer Barcelona, España**Quienes somos** · Desde Ferrer queremos impulsar una nueva forma de hacer negocio y de estar en el mundo. Nuestro propósito es generar un impacto positivo en la sociedad. Nuestro negocio no es un fin en sí mismo, sino un medio para generar cambios sociales sustanciales. Somos a ...
-
Quality Assurance Trainee
hace 6 días
Ferrer Barcelona, España**Quienes somos** · Desde Ferrer queremos impulsar una nueva forma de hacer negocio y de estar en el mundo. Nuestro propósito es generar un impacto positivo en la sociedad. Nuestro negocio no es un fin en sí mismo, sino un medio para generar cambios sociales sustanciales. Somos a ...
-
Quality Assurance Engineer
hace 6 días
Bike24 Barcelona, EspañaBarcelona, Dresden · - ab sofort**(Vollzeit / Teilzeit Option, unbefristet, 100% Remote innerhalb Europas möglich)** · Bei BIKE24 ist jede*r für Qualität verantwortlich. Als **Quality Assurance Engineer / QA Engineer - SAP (m/w/d) **wirst Du Teil unseres bestehenden QA-Teams und ...
-
Senior Quality Assurance Officer
hace 6 días
Viatris Barcelona, España1750 Viatris Pharmaceuticals S.L. · At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. · Viatris empowers people worldwide to live healthier at every ...
-
Quality Assurance Manager
hace 23 horas
Almirall Sant Andreu, EspañaFecha: 15 may Ubicación: SAB0 - PHARMA SANT ANDREU DE L**Misión**: · Asegurar que los Sistemas de Calidad de las plantas farmacéuticas de producción cumplen con las GMPs y las políticas de Calidad Corporativas de Almirall con el fin de garantizar la seguridad, eficacia y calidad ...
-
Quality Assurance Technician
hace 1 semana
Almirall Sant Andreu, EspañaFecha: 22 nov Ubicación: SAB0 - PHARMA SANT ANDREU DE L**Misión**: · Asegurar que los Sistemas de Calidad de las plantas farmacéuticas de producción cumplen con las GMPs y las políticas de Calidad Corporativas de Almirall con el fin de garantizar la seguridad, eficacia y calidad ...
-
Quality Assurance Manager-barcelona
hace 6 días
NonStop Consulting Barcelona, EspañaEstoy trabajando con un centro tecnologico en Barcelona y buscan a un Quality Assurance Manager para uno de sus nuevos proyectos, el proyecto es bastante interesante y trabaja con terapias avanzadas y en el que ademas de haber muy buen ambiente y buena carga de trabajo todos los ...
-
Quality Assurance Trainee
hace 1 semana
Ferrer Sant Feliu de Llobregat, España**Quienes somos** · Desde Ferrer queremos impulsar una nueva forma de hacer negocio y de estar en el mundo. Nuestro propósito es generar un impacto positivo en la sociedad. Nuestro negocio no es un fin en sí mismo, sino un medio para generar cambios sociales sustanciales. Somos a ...
-
Quality Assurance/regulatory Affairs Jr
hace 1 día
BRILL PHARMA Barcelona, EspañaEn dependencia de Dirección Técnica para integrarse en el Departamento Técnico de la compañía, estamos buscando un: Quality Assurance (QA) / Regulatory Affairs (RA) Junior Technician · **Responsabilidades**: · - Dar soporte a los Departamentos de Garantía de Calidad (QA) y de Asu ...
-
Quality Assurance
hace 1 día
Ambit BST Barcelona, España De jornada completa¿Buscas un nuevo reto en un entorno dinámico, colaborativo y de aprendizaje constante? · Si te identificas con la excelencia y el trabajo de calidad, Este es tu sitio · ¿Qué te vas a encontrar? · Compañerismo: Estarás acompañado de un equipo joven, con una calidad humana y profe ...
-
Serialization & Csv Quality Assurance (Pharma)
hace 1 semana
Ambit BST Barcelona, EspañaSi tienes experiência en **serialización y validación de sistemas informáticos** y además te importa generar un impacto positivo en la sociedad, esta vacante es para ti · A través nuestro podrás participar en proyectos de** Quality Assurance **dentro de un importante laboratorio ...
-
Quality Assurance
hace 1 semana
IOMED Medical Solutions Barcelona, EspañaAbout the job · We're looking for a seasoned Quality Assurance Professional to help us accomplish our mission to improve clinical research. Here's what you need to know about the role, our team, and why IOMED is the right next step in your career. · About you · You're an Operatio ...
-
Quality Assurance Coordinator
hace 3 días
Talent Search People Sant Celoni, España**Where will you work?**: · Trabajarás en Uquifa, empresa dedicada a la fabricación de principios activos APIs con presencia internacional y fábrica en Sant Celoni. · **What will you do?**: · - Como Quality Assurance Coordinator darás seguimiento a las tareas de documentación y r ...
-
Quality Assurance Coordinator
hace 1 semana
BSP executive Sant Celoni, España**¿Dónde trabajarás?**: · Trabajarás en Uquifa, empresa dedicada a la fabricación de principios activos APIs con presencia internacional y fábrica en Sant Celoni. · **¿Qué harás?**: · - Como Quality Assurance Coordinator darás seguimiento a las tareas de documentación y registro ...
-
Técnico Quality Assurance
hace 6 días
Lucta Barcelona, España¿Listo para ser un pilar en la excelencia de la calidad alimentaria? Únete como Técnico en Quality Assurance y contribuye a crear un futuro de excelencia. Si estás comprometido con la calidad y la seguridad alimentaria, queremos conocerte. ¿Estás preparado para ser parte del camb ...
-
Supplier Quality Assurance
hace 1 semana
Tobar Talent Solutions Caldes de Montbui, EspañaNuestro cliente es una empresa del sector industrial, ubicada en la comarca de Vallés Oriental, esta buscando un Supplier Quality Assurance que tenga entre uno y dos años de experiência aproximados y que tenga ganas de aprender y desarrollarse en un sector industrial. · MISIÓN · ...
Associate Director, Development Unit Clinical Quality Assurance - Barcelona, España - Novartis Farmacéutica, S. A.
Descripción
Associate Director, Development Unit Clinical Quality Assurance - YS-313 Barcelona, Catalonia Associate Director, Development Unit Clinical Quality Assurance - YS-313Barcelona
Barcelona, Catalonia, ES
392967BRAssociate Director, Development Unit Clinical Quality AssuranceSpainAbout the roleLocation:
Barcelona or Madrid (Hybrid)You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globeAs our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will provide strategic Quality oversight on the entire Clinical Trial Process (CTP) for the clinical trials under responsibility in order to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to Patients' safety, rights and well-being.
This role reports to the Global Head, Development Unit CQA Programs.Your responsibilities will include, but are not limited to:
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
Sufficient years of proven experience in managing projects.Ability to effectively interact with and present to senior management at all levels, as well as to external audiences and inspectors.
Strong skills in GCP, quality and/or clinical development.What you'll receive:
Competitive Salary, Company Pension Plan, Life and Accidental Insurance, Flexible working hours, Hybrid working model, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world.
How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions.Be a part of this mission and join us Learn more here:
our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: UnitQA GDDWork LocationBarcelona Gran VíaCompany/Legal EntityNovartis Farmacéutica, S.
A.Functional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNoEarly TalentNoBack392967BRAssociate Director, Development Unit Clinical Quality AssuranceSpainAbout the roleLocation:
Barcelona or Madrid (Hybrid)You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globeAs our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will provide strategic Quality oversight on the entire Clinical Trial Process (CTP) for the clinical trials under responsibility in order to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to Patients' safety, rights and well-being.
This role reports to the Global Head, Development Unit CQA Programs.Your responsibilities will include, but are not limited to:
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
Sufficient years of proven experience in managing projects.Ability to effectively interact with and present to senior management at all levels, as well as to external audiences and inspectors.
Strong skills in GCP, quality and/or clinical development.What you'll receive:
Competitive Salary, Company Pension Plan, Life and Accidental Insurance, Flexible working hours, Hybrid working model, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world.
How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions.Be a part of this mission and join us Learn more here:
our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: UnitQA GDDWork LocationBarcelona Gran VíaCompany/Legal EntityNovartis Farmacéutica, S.
A.Functional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNoEarly TalentNo392967BRAssociate Director, Development Unit Clinical Quality AssuranceSpainAbout the roleLocation:
Barcelona or Madrid (Hybrid)You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globeAs our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will provide strategic Quality oversight on the entire Clinical Trial Process (CTP) for the clinical trials under responsibility in order to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to Patients' safety, rights and well-being.
This role reports to the Global Head, Development Unit CQA Programs.Your responsibilities will include, but are not limited to:
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
Sufficient years of proven experience in managing projects.Ability to effectively interact with and present to senior management at all levels, as well as to external audiences and inspectors.
Strong skills in GCP, quality and/or clinical development.What you'll receive:
Competitive Salary, Company Pension Plan, Life and Accidental Insurance, Flexible working hours, Hybrid working model, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world.
How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions.Be a part of this mission and join us Learn more here:
our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: UnitQA GDDWork LocationBarcelona Gran VíaCompany/Legal EntityNovartis Farmacéutica, S.
A.Functional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNoEarly TalentNoShare392967BRAssociate Director, Development Unit Clinical Quality AssuranceSpainAbout the roleLocation:
Barcelona or Madrid (Hybrid)You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globeAs our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will provide strategic Quality oversight on the entire Clinical Trial Process (CTP) for the clinical trials under responsibility in order to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to Patients' safety, rights and well-being.
This role reports to the Global Head, Development Unit CQA Programs.Your responsibilities will include, but are not limited to:
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Broad understanding of global expectations of Health Authorities in the area of Clinical Development and profound understanding of the science of product development.
Sufficient years of proven experience in managing projects.Ability to effectively interact with and present to senior management at all levels, as well as to external audiences and inspectors.
Strong skills in GCP, quality and/or clinical development.What you'll receive:
Competitive Salary, Company Pension Plan, Life and Accidental Insurance, Flexible working hours, Hybrid working model, subsidized dining facilities, Employee recognition scheme, learning and development opportunities.
Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world.
How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions.Be a part of this mission and join us Learn more here:
our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: UnitQA GDDWork LocationBarcelona Gran VíaCompany/Legal EntityNovartis Farmacéutica, S.
A.Functional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNoEarly TalentNo392967BRAssociate Director, Development Unit Clinical Quality AssuranceSpainAbout the roleLocation:
Barcelona or Madrid (Hybrid)You will be joining a team of 40 highly talented CQA professionals who are based in various countries across the globeAs our Associate Director, Development Unit CQA (Clinical QA) Program Lead, you will provide strategic Quality oversight on the entire Clinical Trial Process (CTP) for the clinical trials under responsibility in order to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to Patients' safety, rights and well-being.
This role reports to the Global Head, Development Unit CQA Programs.Your responsibilities will include, but are not limited to: