Regulatory Compliance and Deputy Qualified Person
Join to apply for the Regulatory Compliance and Deputy Qualified Person role at Merck Healthcare
Regulatory Compliance and Deputy Qualified Person
Join to apply for the Regulatory Compliance and Deputy Qualified Person role at Merck Healthcare
Aplica tu Magia con nosotros
Estás listo para explorar, romper barreras y descubrir mucho más? Sabemos que tienes grandes planes. Nosotros, también, innovar con la ciencia y la tecnología para enriquecer la vida de las personas con las soluciones en Healthcare, Life Science y Electronics apasiona a nuestros colegas en el mundo entero. Juntos, soñamos en grande y compartimos el entusiasmo por cuidar a una gran diversidad de personas, clientes, pacientes y al planeta. Por eso, siempre buscamos mentes curiosas que imaginen lo nunca visto con nosotros.
Unidos como uno solo para los pacientes : nuestra meta en Healthcare es ayudar a crear, mejorar y prolongar vidas. Creamos tratamientos, dispositivos inteligentes y tecnologías innovadoras en campos terapéuticos como la oncología, la neurología y la fertilidad. Nuestros equipos colaboran en 6 continentes con pasión y una curiosidad incesante con el objetivo de ayudar a los pacientes en cada etapa de su vida. Unirte a nuestro equipo de Healthcare significa formar parte de una cultura de trabajo diversa, inclusiva y flexible, que ofrece fantásticas oportunidades para el desarrollo personal y profesional en todo el planeta.
Your Role : As Deputy Qualified Person and Site Regulatory expert of manufacturing site in Madrid (Tres Cantos ), you will assure that products are manufactured and tested in compliance with GMP requirements and Marketing Authorizations. You will play a pivotal role in coordinating projects, submission strategies and implementation of changes considering scientific and technical progress.
Who You Are
* You hold a university degree in pharmacy.You bring at least 5 years of experience as Qualified Person and / or Regulatory Affairs field.You have a deep understanding of GMP (Good Manufacturing Practices) and quality systems within pharmaceutical manufacturing.
* Your knowledge of applicable EU and highly regulated countries regulations is current and comprehensive.You are comfortable taking legal responsibility for batch release in compliance with EU directives and applicable quality standards.Your strong stakeholder management and communication skills enable you to navigate complex environments effectively.
* You excel at time management, gaining alignment, and executing strategic activities successfully.You prioritize competing tasks effectively in a fast-paced, dynamic environment.You have a strong ability to resolve conflicts constructively and maintain a solution-oriented mindset.
* You are a proactive driver of change-someone who takes initiative and ensures things get done
* You are fluent in both Spanish and English.our advanced skills in standard MS Office and SAP system.
Lo que ofrecemos : Somos mentes curiosas que provienen de una amplia gama de antecedentes, perspectivas y experiencias de vida. Creemos que esta variedad impulsa la excelencia y la innovación, fortaleciendo nuestra capacidad para liderar en ciencia y tecnología. Estamos comprometidos a crear acceso y oportunidades para que todos se desarrollen y crezcan a su propio ritmo. Únete a nosotros para construir una cultura de inclusión y pertenencia que impacte a millones y empodere a todos para defender el progreso humano.
Aplica ahora y conviértete en parte de un equipo que se dedica a Despertar el Descubrimiento y Elevar a la Humanidad!
Seniority level
Seniority level
Associate
Employment type
Employment type
Full-time
Job function
Job function
Quality Assurance and Science
Industries
Pharmaceutical Manufacturing
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