Engineering Validation Specialist

1 Year ago • 2 Years + • Software Development & Engineering

Job Summary

Job Description

Haleon, a global leader in consumer healthcare, is seeking an Engineering Validation Specialist in Panama City. The primary purpose of this role is to ensure the qualification and validation of production equipment, facilities, and systems, guaranteeing their safe use and compliance with regulatory, quality, and safety standards. You will be a key part of a multidisciplinary team driving continuous improvement and operational excellence. Responsibilities include preparing and executing qualification protocols (DQ, IQ, OQ, PQ, FATs), coordinating equipment maintenance and qualifications, collaborating on projects, participating in self-audits, and managing change control meetings.
Must have:
  • Degree in Mechanical, Electromechanical, Industrial, or Chemical Engineering.
  • Minimum 2 years of experience in validation/qualification.
  • Knowledge of GMP, GLP, ISO, USP standards.
  • Proficiency in MS Office (Excel, Word, PowerPoint).
  • Commitment to Health, Safety, and Environment standards.
Good to have:
  • Technical degree in Industrial Mechanics with Electromechanics emphasis.
  • Basic AutoCAD knowledge.
  • Experience in manufacturing processes, automation, and SOPs.
  • Intermediate English level.

Job Details

Somos Haleon, una empresa líder mundial en el cuidado de la salud para nuestros consumidores. Juntos, estamos mejorando la salud cotidiana de millones de personas a través de nuestro portafolio de marcas que combinan el profundo conocimiento humano con ciencia confiable. Algunas de ellas son Corega, Sensodyne, Alikal, Uvasal, Ibuevanol, Hinds, Centrum, Voltaren, Advil y muchas más a nivel global.

Especialista de Validaciones de Ingeniería

Ubicación: Ciudad de Panamá

Modalidad: Presencial | Lunes a Sabado, 8:00 a.m. – 5:00 p.m.

¿Cuál será tu misión?

Tu principal propósito será asegurar la calificación y validación de equipos, instalaciones y sistemas productivos, garantizando su uso seguro y cumplimiento con normativas regulatorias, de calidad y de seguridad. Formarás parte clave de un equipo multidisciplinario que impulsa la mejora continua y la excelencia operativa.

Principales responsabilidades

  • • Elaborar y ejecutar protocolos de calificación (DQ, IQ, OQ, PQ, FATs) de equipos, instalaciones y servicios, asegurando el cumplimiento de normas GMP y estándares internos de calidad y seguridad.
  • • Coordinar la ejecución de mantenimientos y calificaciones de equipos de laboratorio, incluyendo la gestión documental, revisión de reportes y seguimiento con proveedores externos.
  • • Colaborar en proyectos con múltiples áreas aportando criterios técnicos para la correcta validación de equipos y procesos productivos bajo condiciones GMP.
  • • Participar en autoauditorías, investigaciones de desvíos y gestión de acciones correctivas (CAPAs), incluyendo cronogramas e indicadores de cumplimiento.
  • • Verificar condiciones seguras durante operaciones de contratistas y generar reportes de seguridad.
  • • Participar activamente en reuniones de cambio de control, brindando criterios técnicos sobre impacto en estado calificado o validado de los procesos.
  • • Gestionar cierres de CAPAs, actualizaciones de SOPs, documentación GMP y acciones de cumplimiento según requerimientos del área.
  • • Asumir cualquier otra tarea asignada por la Gerencia que contribuya al cumplimiento de los objetivos del área.

¿Por qué TÚ?

Tus calificaciones:

  • • Profesional graduado en Ingeniería Mecánica, Electromecánica, Industrial, Química o carreras afines. También se considera formación técnica como Bachiller Industrial con énfasis en Electromecánica.
  • • Mínimo 2 años de experiencia en validaciones, calificación de equipos o procesos dentro de industrias reguladas.
  • • Conocimiento en normativas internacionales (GMP, GLP, ISO, USP) y herramientas de análisis estadístico y documentación regulatoria.
  • • Manejo intermedio de MS Office (Excel, Word, PowerPoint); conocimientos básicos de AutoCAD son un plus.
  • • Nivel de inglés intermedio.
  • • Experiencia en procesos de manufactura, automatización de equipos y uso de SOPs.
  • • Compromiso con los estándares de Salud, Seguridad y Medio Ambiente.

¿Estás listo para marcar la diferencia en la salud cotidiana de millones de personas?

Postúlate ahora y forma parte de una compañía donde el crecimiento profesional y el propósito van de la mano.

Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/

At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.

Haleon is an Equal Opportunity 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.

Accommodation Requests

If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific accommodations you are requesting. We’ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.

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About The Company

Hello. We’re Haleon. A new world-leadingconsumer healthcarecompany. Shaped by all of us. Together, we’re improving everyday health for millions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol,Advil, Voltaren,Theraflu, Otrivin,and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re building together. In anenvironment thatwe’re co-creating. And a culture that’s uniquely ours. Care to join us.

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