305 Ofertas de Pfizer en España

Quality Assurance Trainee

Location: O Grove (hybrid)

Department: Quality Assurance

Position type: Internship

At Bolton Food, we are looking for a Quality Assistant Intern to join our Quality Department. This role is a great opportunity to support key quality and packaging projects while gaining a comprehensive view of our operations. You will work closely with different departments, collaborate with suppliers and marketing teams, and actively contribute to process improvements and quality assurance initiatives across our plants.

What are you going to do

• Support and collaborate in packaging project management, collaborating with the Marketing department, design agencies, and suppliers (cans, boxes, cartons).
• Assist in the creation and approval of product labels, packaging data sheets, and product specifications.
• Collaborate in outsourcing activities for packaging and quality follow-up.
• Learn and gain a global understanding of plant operations (Grove and Cabo de Cruz).
• Help with material code creation and maintenance in SAP.
• Work alongside different departments to support quality alignment.
• Contribute to process improvement, time reduction, and waste minimization.
• Assist in continuous improvement initiatives related to Quality Assurance.

What we are looking for

Education: Degree or Master’s Degree in Food Technologies, Chemistry or similar.

Technical skills: Suite Office (Word, Power Point, Excel).

Languages: Proficient in Spanish and English, other languages such as French or Italian will be positively valued.

Personal profile:

• A motivated young neo-professional eager to grow and evolve professionally.
• A proactive and fast learner keen to evolve, challenging himself/herself daily in order to reach excellence and focus on customers and stakeholders satisfaction.
• A fully accountable and an effective communicator, able to instill trust and build meaningful relationships with internal and external stakeholders.
• A dynamic, resilient and flexible professional capable to adapt swiftly and manage a fast moving and demanding environment.

What’s interesting for you

An opportunity to discover and learn from a leading company in the food industry.

Professional growth & development within a dynamic and evolving environment.

A key supportive role in Quality Department, where your freshness of ideas will directly impact the evolution of our Quality Department.

Curiosity on Bolton

Bolton is a multinational family-owned company that enriches the hearts and homes of families worldwide with trusted brands. Present in over 150 countries, it employs 11,000 people in 55 offices, 17 factories, and 8 R&D laboratories. We foster growth in a culture where everyone collaborates and embraces the entrepreneurial spirit.

About Bolton Food

Bolton Food and Tri Marine is the Bolton business unit responsible for activities across the food supply chain. This includes managing a fleet of fishing vessels and promoting increasingly sustainable fisheries (alongside WWF and OXFAM) that prioritize marine ecosystem protection and surrounding communities. Production takes place through a network of 10 specialized industrial plants worldwide. Through flagship brands like Cuca, Isabel, Rio Mare , and Saupiquet , the business unit also markets tasty, innovative, and carefully prepared food products enjoyed by millions of families worldwide.

At Bolton Group, we value and celebrate diversity. Bolton Group is committed to equal employment opportunities and prohibits any form of discrimination. Connect with us to learn more about Bolton Group.

#BoltonFood

¿Buscas un nuevo reto para continuar desarrollando tu carrera profesional?

En ALTEN España estamos seguros que conocer y superar las expectativas de las personas es uno de nuestros secretos para alcanzar el éxito. ¿Quieres ser parte de esto?

Desde la división de Life Sciences nos hemos puesto en marcha y nos gustaría conocer a las personas que estén dispuestas a ser parte del corazón de nuestra empresa.

¿Qué buscamos?

En esta ocasión, buscamos un/a Quality Assurance Specialist para incorporarse a una planta farmacéutica ubicada en Girona.

¿Qué tipo de funciones podrás realizar?

• Elaboración y revisión de documentación de validación y protocolos de cualificación (IQ/OQ/PQ), asegurando su correcta ejecución según normativas GMP.
• Soporte en la preparación y desarrollo de inspecciones de autoridades sanitarias, garantizando el cumplimiento de los requisitos regulatorios.
• Gestión y consulta de documentación técnica y de calidad mediante herramientas como VEEVA , asegurando trazabilidad y control documental durante todo el proceso.

¿Qué esperamos de ti?

• Experiencia previa en entornos GMP dentro de la industria farmacéutica.
• Conocimientos sólidos en cualificación de equipos (IQ/OQ/PQ) y validaciones de proceso.
• Experiencia en líneas de granulación vía húmeda y en la gestión documental en sistemas tipo VEEVA.
• Capacidad de integración en equipos multidisciplinarios y orientación al detalle
• Disponibilidad para trabajar de forma presencial en Girona, España.

¿Qué te espera en nuestro equipo de ALTEN España?

• Tendrás la oportunidad de participar en proyectos de alto nivel tecnológico e innovador.
• Planes de formación profesional gracias a nuestros cursos diseñados para apoyarte en el crecimiento de tus habilidades técnicas sectoriales y lingüísticas.
• Acceso iniciativas y programas diseñados para el bienestar de las personas.

Así que ya sabes, ¡haznos llegar tu perfil y estaremos encantados de conocerte!

Ubicación: Benniel (Murcia)

¿Quiénes somos?

HTBA es un líder global basado en la ciencia en la fabricación y comercialización de flavonoides cítricos y formas activas de vitamina B12, destinados a los sectores nutracéutico, farmacéutico, alimentario, de bebidas y nutrición animal. Durante más de cuarenta y cinco años, la empresa ha sido pionera en el desarrollo de nuevos procesos para crear ingredientes de alta calidad y origen natural que promueven la salud de las personas y los animales, todo ello protegiendo al mismo tiempo el medio ambiente.

Con sede en Barcelona, HTBA produce ingredientes de calidad inigualable en su moderna planta de fabricación ubicada en Murcia, España. Además, con centros de innovación situados en España y en su centro de operaciones en América del Norte, en Ohio, la empresa está estratégicamente posicionada para comprender y responder rápidamente a la demanda global de los consumidores finales.

OBJETIVO DE LAS PRÁCTICAS

El objetivo principal de las prácticas es introducir al estudiante en el entorno industrial farmacéutico, proporcionándote formación práctica en distintas disciplinas clave como la Garantía de Calidad, el Control de Calidad y los procesos productivos.

CONOCIMIENTOS QUE ADQUIRIRÁS

Durante tu estancia en el departamento de Garantía de Calidad adquirirás conocimientos y experiencia práctica en:

• Fundamentos de los sistemas de calidad en la industria farmacéutica.
• Procesos de fabricación y su documentación asociada.
• Procedimientos de calidad.
• Gestión documental, revisión de guías de fabricación y procesos de calidad.
• Normativas GMP (Good Manufacturing Practices) y su aplicación práctica.

PROYECTO/ FUNCIONES A REALIZARÁS

Colaborarás en las siguientes tareas y funciones dentro del departamento:

• Apoyo en la revisión documental.
• Colaboración en la gestión y seguimiento de desviaciones, OOS y CAPAs.
• Apoyo en la actualización y control de versiones de documentación GMP.
• Participación en tareas de archivo y control de registros.

PERFIL PREFERENTE

Formación académica: Ciencias

Formación específica: Química/ Farmacia

Idiomas: Inglés nivel intermedio

Main responsibilities:

• Review requirements, specifications, and technical design documents to provide timely and meaningful feedback before building.
• Create detailed, comprehensive, well-structured test plans and cases to structure the testing process.
• Provide estimates, prioritize, plan and coordinate testing activities to align with the development cycle.
• Design, develop and execute automation scripts using open-source tools.
• Identify, record, document thoroughly, of things that are not working well so that developers can work effectively to resolve them.
• Perform thorough regression testing to check that bugs or fixes are appropriately resolved.
• Take a user-centered approach and make sure that requirements and tests cover the right things so the results are usable and in line with UX Standards.
• Liaise with internal teams (e.g. developers, product managers, product owners, Digital Quality) to identify system requirements, including those required to meet applicable quality, regulatory (Data Privacy, GxP, SOX, etc.) and cybersecurity standards.
• Track quality assurance metrics, like defect densities and open defect counts.

Key Skills:

• Experience in behavioural testing of the user experiences.
• Automated testing tools and automated test script development.
• DevOps and DevOps Tools such as JIRA, X-Ray, Confluence, etc.
• Agile Mindset and Practices, and working as part of the SCRUM team
• Experience testing single page applications with complex user flows.
• It would be nice to have experience with SAP e-commerce, SAP Hybris or SAP Commerce Cloud, and integration with other systems.

Main responsibilities:

• Review requirements, specifications, and technical design documents to provide timely and meaningful feedback before building.
• Create detailed, comprehensive, well-structured test plans and cases to structure the testing process.
• Provide estimates, prioritize, plan and coordinate testing activities to align with the development cycle.
• Design, develop and execute automation scripts using open-source tools.
• Identify, record, document thoroughly, of things that are not working well so that developers can work effectively to resolve them.
• Perform thorough regression testing to check that bugs or fixes are appropriately resolved.
• Take a user-centered approach and make sure that requirements and tests cover the right things so the results are usable and in line with UX Standards.
• Liaise with internal teams (e.g. developers, product managers, product owners, Digital Quality) to identify system requirements, including those required to meet applicable quality, regulatory (Data Privacy, GxP, SOX, etc.) and cybersecurity standards.
• Track quality assurance metrics, like defect densities and open defect counts.

Key Skills:

• Experience in behavioural testing of the user experiences.
• Automated testing tools and automated test script development.
• DevOps and DevOps Tools such as JIRA, X-Ray, Confluence, etc.
• Agile Mindset and Practices, and working as part of the SCRUM team
• Experience testing single page applications with complex user flows.
• It would be nice to have experience with SAP e-commerce, SAP Hybris or SAP Commerce Cloud, and integration with other systems.

Join Our Team as a QA Tester at Ibancar

Ibancar is an innovative fintech business in the online lending / consumer credit sector that operates in Spain and is expanding to Mexico. The business is one of the fastest growing VC backed scale-ups in Spain and is revolutionizing digital lending through the use of cars as collateral. Ibancar applies a fully digital onboarding and approval process for borrowers and offers same day loans that are ethical, inclusive and accessible.

We are currently looking for an ambitious and highly motivated Developer to join our dynamic team to help adapt our platform, tech stack and work processes to launch Ibancar in Spain-México.

This is a demanding but fulfilling job presenting a unique opportunity to join a very ambitious business. It will be a very hands-on role and ideally the successful candidate will have worked previously for a fintech or financial business in Spain.

The successful candidates MUST:

Speak Spanish and English Intermediate.

Have demonstrable project experience in a relevant sector.

Have experience in QA and fully responsive web development.

Have several years experience of working in a startup or fast growing business environment.

This position is based in Málaga, Spain

What´s your story?

• 2+ years experience in software testing
• Strong knowledge of test methodologies QA and SQL best practices.
• Experience with JavaScript, PHP (Laravel or similar), Vue.JS, HTML, CSS, Jira.
• Basic programming skills for test automation.
• Experience testing RESTful web services and API's-Postman
• Excellent communication and analytical skills

Why Join Us?

You will be part of a growing company with an inclusive work environment full of exciting challenges.

You will actively participate in transforming the fintech industry, with access to advanced resources and a culture that values innovation and excellence.

We offer a modern and flexible startup culture, a great work environment and an exciting career path with uncapped potential.

To apply for this exciting opportunity, please send your CV highlighting your relevant experience and why you're passionate about joining Ibancar to

In a few words

Position: Quality Assurance Technician

Location: Valencia

Experience: + 2 years

Global Responsibility

Ensure the quality of processes and take the necessary measures to ensure that products manufactured meet the Good Manufacturing Practices. Investigate deviations, complaints and OOS in order to propose corrective actions and improvements. Research and ensure corrective and preventive as a result of claims, customer audits. Ensure continuous improvement and maintenance of quality of equipment, systems and processes. Comply with the guidelines defined in the Quality Policy, Objectives of the company and with regulations and quality standards of organisms .

Specific Responsibilities

• Review specifications of bulk biopharmaceutical products.
• Review and approve all master batch records and oversee computer system validation (e.g., SAP) to enable manufacturing processes.
• Create and maintain Hazard Analysis and Critical Control Point (HACCP) documentation, adapted to pharma processes and products.
• Collaborate as needed to ensure all client requirements and requests related to pharmaceutical products are addressed.
• Coordinate the Quality System and serve as the main customer contact for pharma products.
• Develop procedures and analytical specifications for bulk biopharmaceutical products.
• Review documentation for raw materials, bulk, and finished biopharmaceutical products.
• Manage Change Control processes for pharma products.
• Manage complaints related to pharma products.
• Manage deviations related to pharma products.
• Oversee supplier management: approve and evaluate suppliers, and review and approve all supplier documentation relevant to pharma.
• Collaborate in the performance of audits for contract manufacturing organizations (CMOs) in the pharma sector.
• Collaborate in the performance of supplier quality audits specific to pharma.
• Participate as a member of the shelf inspections audit team for biopharmaceutical products.
• Collaborate in the management of Customer Quality Audits performed on site for pharma products.
• Manage CAPA (Corrective and Preventive Actions) resulting from Customer Quality Audits, Complaints, Deviations, and OOS (Out of Specification) findings in the pharma context.

Competencies/Career Level

Innovation, customer orientation, communication, teamwork, adaptability/flexibility, productivity, Self-development, sense of urgency, Initiative.

Requirements and personal skills

• Education: Bachelor Degree in Sciences.
• Languages: High level of English and Spanish.
• Experience (years/area): +2
• Specific Knowledge: Quality Assurance experience. SAP Management, MS Office system.
• Travels: Willing to travel occasionally.
• Personal skills: Good communication skills, proactivity, good working under pressure, problem-solving, good organizational skills and persistent.

QA Lead – Nuitée (Barcelona, Dublin, London or Casablanca or Remote EU)

About Nuitée

Nuitée is building the API infrastructure of the global travel industry — a scalable platform that enables OTAs, fintechs, banks, and super-apps to access hotel inventory in real time, with better pricing and coverage.

We’re trusted by major players like Google, Uber, Hopper, and Expedia , and backed by leaders from Airbnb, Meta, Hotelbeds, and Sabre . As we scale rapidly, we’re looking for a QA Lead to own and evolve our quality assurance strategy across the product and engineering org.

Your Mission

As QA Lead, you will be the first dedicated QA owner at Nuitée. This role is perfect for someone who thrives as a hands-on individual contributor (IC) and wants to lay the foundations for a best-in-class QA culture. You’ll define the strategy, build automation, and ensure the reliability of our core platform.

¿Buscas un nuevo reto para continuar desarrollando tu carrera profesional?

En ALTEN España estamos seguros que conocer y superar las expectativas de las personas es uno de nuestros secretos para alcanzar el éxito. ¿Quieres ser parte de esto?

Desde la división de Life Sciences nos hemos puesto en marcha y nos gustaría conocer a las personas que estén dispuestas a ser parte del corazón de nuestra empresa.

¿Qué buscamos?

En esta ocasión, buscamos un/a Quality Assurance (GDP) para unirse a un equipo internacional asumiendo un rol clave en proyectos dentro del sector farmacéutico.

En este rol como Quality Assurance (GDP) , tendrás la oportunidad de asegurar el cumplimiento de las Buenas Prácticas de Distribución (GDP) y apoyar las actividades globales relacionadas con la gestión de calidad, cualificación de transportes (especialmente cadena de frío) y mejora continua en los procesos de distribución.

¿Qué tipo de funciones podrás realizar?

Gestión de calidad en Supply Chain global

• Soporte en la gestión de temas globales de calidad en la cadena de suministro.
• Coordinación y seguimiento de problemas de transporte de producto en colaboración con los equipos regionales y globales.
• Gestión y revisión de investigaciones de distribución, desviaciones y acciones CAPA.
• Impulso de iniciativas de mejora continua y formación en temas de calidad.
• Supervisión y optimización de los procesos globales de Serialización y Artwork Management.
• Revisión y soporte en acuerdos técnicos de calidad (TQA) con fabricantes contratados (FF) y proveedores logísticos (LSP).
• Participación en Quality Management Reviews (QMRs) y seguimiento de KPI y dashboards de calidad.
• Monitoreo de la evolución regulatoria y soporte en la implementación de nuevos requisitos.
• Redacción, revisión y mantenimiento de SOPs globales.

Soporte en cualificación de transporte (especialmente cadena de frío)

• Participación en evaluaciones de riesgo y mapeo de rutas con FF y LSP.
• Revisión y aprobación de protocolos y reportes de cualificación de transporte.
• Evaluación de riesgos, comunicación de resultados y seguimiento de CAPAs.
• Validación y mejora continua mediante revisiones periódicas de riesgos.

¿Qué esperamos de ti?

• Experiencia mínima de 5 años en entornos GMP/GDP, preferiblemente en la industria farmacéutica o logística asociada.
• Conocimientos sólidos en cualificación de transportes y cadena de frío.
• Experiencia en la gestión de CAPAs, desviaciones, control de cambios y documentación GDP.
• Nivel de inglés intermedio (B2). Es un plus un tercer idioma como francés.
• Manejo avanzado de Power BI, Trackwise y sistemas QMS.
• Disponibilidad para trabajar de forma híbrida 50/50 en Barcelona, España.

¿Qué te espera en nuestro equipo de ALTEN España?

• Tendrás la oportunidad de participar en proyectos de alto nivel tecnológico e innovador.
• Planes de formación profesional gracias a nuestros cursos diseñados para apoyarte en el crecimiento de tus habilidades técnicas sectoriales y lingüísticas.
• Acceso iniciativas y programas diseñados para el bienestar de las personas.

Así que ya sabes, ¡haznos llegar tu perfil y estaremos encantados de conocerte!

#ALTENSpain #LifeSciences