Haleon
Consumer Health
EspecialistadeValidacionesdeIngienería(Temporal)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Especialista de Validaciones de Ingienería (Temporal) at Haleon. Skills: Validation, Qualification, GMP compliance. Elaborate and execute qualification protocols. Coordinate equipment maintenance and qualification”
Industry & Context.
Deviation investigations; Root cause analysis
What They're Looking For.
Must Have
Professional graduated in Engineering, Minimum 2 years experience, Knowledge in international regulations, Knowledge in quality systems, Intermediate MS Office, Intermediate English level, Experience in manufacturing processes, Experience in equipment automation, Experience in SOPs use, Commitment to HSE standards
Nice to Have
Basic AutoCAD knowledge
What You'll Do.
Elaborate and execute qualification protocols
Coordinate equipment maintenance and qualification
Manage laboratory equipment documentation
Review protocols and reports
Follow up with external providers
Collaborate in projects
Provide technical criteria for validation
Participate in self-audits
Participate in deviation investigations
Manage corrective and preventive actions
Define CAPA timelines
Define CAPA indicators
Verify safe conditions during contractor activities
Generate unsafe condition reports
Participate in change control meetings
Provide technical criteria on impact
Update GMP documentation
Integrate into multidisciplinary team
Achieve area objectives
Assume assigned tasks
How You'll Work.
Team & Collaboration
Multidisciplinary team
Full Job Description
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. ## ## ¿Cuál será tu misión? Tu principal propósito será realizar y asegurar la calificación y validación de equipos, instalaciones y sistemas productivos, garantizando su uso seguro y el cumplimiento de requisitos regulatorios, de calidad y de seguridad. Formarás parte de un equipo multidisciplinario enfocado en la mejora continua y la excelencia operativa del site. ## Principales responsabilidades • Elaborar y ejecutar protocolos de calificación (DQ, IQ, OQ, PQ, FATs y comisionamiento) de equipos, instalaciones y servicios, asegurando el cumplimiento de normas GMP y estándares internos de calidad, seguridad y medio ambiente. • Coordinar la ejecución de mantenimientos y calificaciones de equipos de laboratorio, incluyendo la gestión documental, revisión de protocolos y reportes, y seguimiento con proveedores externos. • Colaborar en proyectos con diferentes áreas, aportando criterios técnicos para la correcta validación de equipos, sistemas y procesos productivos bajo condiciones GMP. • Participar en autoauditorías, investigaciones de desvíos y gestión de acciones correctivas y preventivas (CAPAs
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