Senior Veeva RIM Consultant - Remote, Impactful Change

Sii Poland; Toruń; A distancia; PLN 90.000 - 140.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Great Place to Work

Profit sharing

Regular integration events

Remote work option

Career development programs

Medical care

Descripción de la vacante

Sii Poland is seeking a Senior Veeva Consultant with deep experience in Veeva Vault and RIM to manage configuration and validation documentation in a GxP environment. This remote role involves collaborating with business stakeholders and Digital QA teams to ensure governance and quality standards are met.

You’ll drive impact analyses, align with governance, and ensure the integrity of validated systems while working on scalable, compliant solutions for the pharmaceutical industry.

Formación

• Experience with Veeva RIM and GxP in pharma environments.
• Proven ability to conduct impact analyses and change control.
• GxP regulations knowledge and validation documentation experience.

Responsabilidades

• Manage configuration and validation docs for system changes in RIM.
• Conduct impact assessments to ensure GxP compliance.
• Gather requirements and design scalable system solutions with stakeholders.
• Oversee end-to-end management of changes from design to validation.
• Collaborate with Digital QA/Enablement teams to translate requirements into solutions.
• Monitor Veeva General Releases and assess release impact.
• Work independently while adhering to governance and quality standards.
• Ensure integrity of validated systems in a regulated environment.

Conocimientos

Veeva RIM

Impact assessments

Change management

Fluent English

Herramientas

Jira Xray

Descripción del empleo

Sii Poland is seeking a Senior Veeva Consultant with deep experience in Veeva Vault and RIM to manage configuration and validation documentation in a GxP environment. This remote role involves collaborating with business stakeholders and Digital QA teams to ensure governance and quality standards are met.

You’ll drive impact analyses, align with governance, and ensure the integrity of validated systems while working on scalable, compliant solutions for the pharmaceutical industry.