Senior Business Analyst, R&D Informatics

Merck Gruppe; Mollet del Vallès; Presencial; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

Une entreprise pharmaceutique de premier plan recherche un Lead Expert en Qualité pour rejoindre son équipe dynamisée. Vous serez responsable de la configuration du système Veeva Vault Quality et de l'amélioration continue des opérations au sein de R&D, tout en jouant un rôle clé dans la gestion de la qualité. Ce poste, adapté à des professionnels passionnés par l'assurance qualité, exige une collaboration avec divers intervenants et une expérience approfondie des outils de gestion réglementaire.

Formación

• Minimum 5 ans d'expérience dans une entreprise pharmaceutique.
• Minimum 3 ans en affaires réglementaires.
• Expérience pratique avec des outils de qualité réglementaire.

Responsabilidades

• Configurer le système Veeva Vault Quality selon les exigences des utilisateurs.
• Documenter des processus et créer des supports de formation.
• Collaborer avec le support technique et les équipes de gestion du changement.

Conocimientos

Gestion de la qualité

Gestion de projet

Analyse problématique

Communication efficace

Educación

Diplôme supérieur dans une discipline scientifique ou expérience équivalente

Herramientas

Outils de gestion de la qualité réglementaire

Microsoft Excel

Descripción del empleo

Your role:Join our dynamic "Veeva Vault Solutions Team" within "DDIT R&D," where you'll be at the forefront of innovation and quality in our pharmaceutical applications. As the Lead Expert in Quality, you'll serve as a crucial link between business needs and IT capabilities, ensuring that our Veeva Vault Quality system is configured to meet the evolving demands of our R&D user community. You'll collaborate with diverse teams to gather and analyze business requirements, translating them into effective system configurations. This role allows you to document processes meticulously and create training materials that empower teams to leverage the Veeva Vault Quality system effectively. You'll work closely with technical support and change management teams to integrate new functionalities seamlessly. Your insights will drive continuous improvement initiatives, enhancing system performance based on user feedback. By joining us, you'll play a pivotal role in shaping the future of our R&D operations, making a tangible impact on quality management. If you are passionate about quality assurance and thrive in a collaborative environment, we want to hear from you!

Who you are:

• You hold a higher degree in a scientific discipline or have equivalent work experience.
• You have at least 5 years of professional experience in a pharmaceutical company or service provider, with a minimum of 3 years in Regulatory Affairs.
• You possess extensive practical experience in regulatory quality management tools, including data governance.
• You have a Veeva White Belt Certification (preferred).
• You bring demonstrated experience in managing system administration support in a regulated environment, including computer systems validation.
• You excel in Microsoft Office, particularly MS Excel, and have strong organizational and planning skills.
• You are known for your strong analytical problem-solving skills and excellent stakeholder management abilities.
• You communicate effectively in English, with German language skills being an asset.

Role: Expert 3

*Todos los candidatos internos, sin importar si trabajan a tiempo completo o parcial, tendrán la oportunidad de ser considerados para las vacantes disponibles