Veeva Administrator - Katalyst Healthcares & Life Sciences
Sommerset, NJ 08873
About the Job
Responsibilities :
- IT System Administration experience for Veeva vault (Quality, RIM, Clinical) REQUIRED and Compliance Wire learning management system PREFERRED.
- Demonstrated experience performing change management/validation activities in support of vendor enhancements and user requirements using validation lifecycle management and electronic signature systems REQUIRED.
- Role Overview.
- The Quality Systems Specialist/Admin will be responsible for maintaining various quality and validation applications.
- IT System Administration/Vault Owner in Veeva vault (Quality, RIM, Clinical), learning management system, validation lifecycle management system, electronic signature systems.
- Perform configuration and change management activities in support of vendor enhancements and customer requirements.
- Participate in the authoring and execution of computerized system validation testing and documentation.
- Liaise with computer system vendors, IT partners, and the business to coordinate implementation activities.
- At least 3 years' experience.
- Pharmaceutical Project experience.
- Proficient knowledge and understanding of Microsoft Office Applications (Access, Excel, Project, PowerPoint, SharePoint, Teams, Word) and/or other relevant software programs.
- Demonstrated ability to work independently to complete assignments within defined time constraints.
- Ability to interpret and apply GxPs, regulatory requirements, Computer Systems Validation (CSV), SDLC, and industry best practices.
- Self-directed with a high degree of professional integrity, very organized, and detail-oriented.
- Validation Lifecycle Management System (ValGenesis, Client ALM, etc.), Change control, document management systems (Veeva, Documentum, etc.), DocuSign/Adobe Sign.
Source : Katalyst Healthcares & Life Sciences
