Senior Business Analyst, R&D Informatics

Merck Group; Barcelona; Presencial; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

Join Merck Group as a Lead Expert in Quality within the Veeva Vault Solutions Team, where you'll enhance pharmaceutical applications. This role involves ensuring quality management through effective system configuration and collaboration, impacting R&D operations significantly. Applicants should have a higher degree in a scientific field and extensive experience in regulatory quality management, contributing to innovative solutions.

Formación

• 5+ years of professional experience in a pharmaceutical company or service provider.
• Experience in Regulatory Affairs (minimum 3 years).
• Demonstrated system administration support in a regulated environment.

Responsabilidades

• Gather and analyze business requirements for Veeva Vault Quality system.
• Document processes and create training materials.
• Drive continuous improvement initiatives based on user feedback.

Conocimientos

Analytical problem-solving

Stakeholder management

Data governance

Collaboration

Educación

Higher degree in a scientific discipline

Herramientas

Microsoft Office

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

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