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Veeva Administrator

RxCloud

RemoteUnited StatesmidFull Time
Posted
3 weeks ago
Source
Himalayas

Skills

Communication

Description

Job description: The Veeva Administrator is responsible for ensuring the Veeva Vault Applications are maintained in a compliant manner. Responsibilities encompass administration of Veeva Vault Regulatory Information Management, document, training, Quality Management, and Laboratory Information Management systems. Experience: min 6 years Responsibilities: - - Serves as the Veeva Business Administrator responsible for the implementation, management, and ongoing maintenance of the Veeva Vault, including documents, training, QMS, LIMS, and RIMs. - Coordinates with business process owners for change control, quality assessment, and approval, testing, and deployment. - Develops and implements ongoing training. - Creates and maintains user accounts. - Ensures controls related to approval levels and user access are established and maintained. - Manages changed static data. - Proactively identifies and works to resolve project and system issues. - Ensures Veeva Vault conforms to regulatory requirements. - Oversees and participates in the development of application documentation. - Ensures system workflows and triggers are developed and maintained as established by business process owners. - Works with business stakeholders to develop and prepare reports, metrics, and dashboards. - Works closely with various business stakeholders to lead and manage business requirements and system solution delivery. - Supports ongoing maintenance and enhancements as required. - Assesses changes to the system (e.g. new releases) for business and training impact. - Drive improvements and efficiencies. Minimum Qualifications (Knowledge, Skills, and Abilities) - A Bachelor's Degree in a related field plus 6 years of Quality, Regulatory, or System Administrator experience, or equivalent work experience is required. - Proven experience in leading and deploying a combination of the following: QMS, document management, Electronic Learning Management System, or Regulatory Information Management System. - Experience in a pharmaceutical or any highly regulated environment is preferred. - Knowledge of Quality Assurance/Quality Control Operations and Regulatory. - Experience with system design and development from business requirements analysis to implementation and support. - Possess and demonstrate excellent oral and written communication skills and proactive problem-solving, analytical, and multi-tasking skills. - Possess the ability to work within a team-based environment while proactively forging positive relationships across all levels of management, departments, and suppliers. - Quality Systems Experience in a CGMP environment - Excellent written/oral communication skills - Self-motivated, flexible, and able to work in a small, fast-paced, dynamic, environment. Originally posted on Himalayas

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