Mlr Process Manager_ Pharma/English

buscojobs España; Sevilla; Presencial; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

Una reconocida empresa farmacéutica busca un MLR Process Manager para optimizar procesos y colaborar con diversas partes interesadas. El rol incluye la gestión de iniciativas de MLR y el desarrollo de planes de información médica, ofreciendo la oportunidad de participar en proyectos internacionales en un entorno dinámico. Se valora la experiencia en herramientas como Veeva Vault y se proporciona un contrato indefinido a través de Hays.

Servicios

Participación en proyectos internacionales

Ambiente joven y dinámico

Horario flexible

Buffet onsite

Contrato a largo plazo via Hays

Formación

• Experiencia mínima de 3 años en Información Médica o Gestión de Publicaciones Médicas.
• Capacidad para interpretar requisitos y desarrollar soluciones efectivas.

Responsabilidades

• Evaluar y optimizar procesos y plataformas de forma continua.
• Apoyar la implementación de iniciativas globales de MLR.

Conocimientos

Fluidez en inglés

Optimización de procesos

Colaboración con stakeholders

Educación

Licenciatura en áreas científicas (farmacia, biología, química)

Máster en gestión científica o similar

Herramientas

Veeva Vault

Descripción del empleo

Hays is collaborating with a leading company in the pharmaceutical sector (founded in 1885), ranked in the TOP 10 pharma companies worldwide.

This company has more than 146 affiliates globally and employs over 52,000 people, including more than 1,600 in Spain. They develop innovative medicines for humans and animals, adding value through innovation across three business areas: human pharmaceuticals, animal health, and contract manufacturing of biopharmaceuticals.

The company is in an expansion phase, focusing on talented and ambitious individuals passionate about innovation. They are establishing a technological hub to serve the entire group globally, located in Barcelona.

We are looking for a MLR Process Manager.

Your role will involve supporting the development and delivery of scientific publications and medical information plans.

Key responsibilities include:

1. Continuous assessment and optimization of end-to-end processes, platforms, and tools (e.g., planning, project tracking, workflows, roles, and responsibilities).
2. Understanding local regulatory requirements for project execution.
3. Collaborating with stakeholders such as Project Owners across regions to gather feedback, provide updates, solve problems, and promote continuous improvement.
4. Supporting the implementation of global MLR initiatives with local adaptations.
5. Identifying and implementing process improvements to enhance review efficiency.
6. Coordinating stakeholder meetings and aligning teams.
7. Developing demand forecasts, asset planning, and resource allocation.
8. Tracking agency performance and maintaining content compliance.
9. Supporting platform changes and guiding teams through transitions.
10. Providing platform training and user support for Vault-related issues.
11. Creating performance reports to inform data-driven decisions.

Requirements:

• Bachelor's degree in science-related fields (pharmacy, biology, chemistry, etc.).
• Master’s degree in a scientific field with education in Operations Management, Process Management, Project Management, Business Administration, or Information Management is highly valued.
• Experience with Veeva Vault.
• Fluent in English (written, reading, speaking).
• Spanish, German, or other languages are a plus but not required.
• At least three years’ experience in Medical Information, Medical Publication Management, or Medical Affairs, to interpret requirements, develop solutions, and communicate effectively.

What we offer:

• Participation in international projects.
• Young and dynamic environment.
• Flexible schedule with 1 office day per month in Barcelona.
• Onsite buffet.
• Long-term contract via Hays (indefinite).

If you are passionate about science and health, we encourage you to apply so we can share more details with you!