puestos de Lider en España

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

Should you require any reasonable adjustments or arrangements to support you during the recruitment process specific to your individual needs please contact us on .

Please note should your enquiry not relate to adjustments we will not be able to support you through these channels.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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 GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at

Ubicación: Aranda de Duero Burgos
Área: MSAT (Manufacturing Science & Technology)
Tipo de contrato: Indefinido

Tus principales responsabilidades

• Actuar como referente técnico en materiales de acondicionamiento primario y secundario para toda la planta.
• Proponer y liderar proyectos de mejora (calidad eficiencia y reducción de residuos). Coordinar y asegurar la correcta ejecución de cualificaciones de equipos y validaciones de procesos manteniendo el estatus de validación.
• Ejecutar y supervisar actividades de verificación continuada de procesos y gestión del ciclo de vida de equipos procesos y productos. Gestionar e implementar cambios y resolver incidencias técnicas.
• Liderar y participar en la gestión de desviaciones y en el establecimiento de estándares de proceso conforme a políticas y requisitos regulatorios.
• Mantener actualizado el repositorio de conocimiento técnico (lecciones aprendidas mejoras documentación). Actuar como apoyo (backup) en otras actividades del departamento según competencias.
• Apoyar en auditorías internas y externas. Colaborar en la transferencia de nuevos productos al área.

Requisitos

• Titulación universitaria en Ingeniería Ciencias o área similar.
• Alto nivel de inglés (oral y escrito).
• Proactividad orientación a resultados y capacidad para trabajar en equipo.
• Experiencia en industria farmacéutica y conocimiento de normativas GMP.

Qué ofrecemos

• Incorporarte a una compañía líder en el sector farmacéutico.
• Entorno dinámico y colaborativo con oportunidades reales de desarrollo profesional.
• Participación en proyectos estratégicos con impacto directo en calidad y eficiencia de procesos.

Fecha límite para aplicar: 26/01/2026

Key Skills

• Lean Manufacturing
• Six Sigma
• Continuous Improvement
• ISO 9001
• Lean Six Sigma
• Management Experience
• Manufacturing & Controls
• 5S
• Manufacturing Management
• Kaizen
• Chemistry
• Manufacturing

Employment Type : Full-Time

Experience: years

Vacancy: 1