Veeva Systems is a missiondriven organization and pioneer in industry cloud helping life sciences companies bring therapies to patients faster. As one of the fastestgrowing SaaS companies in history we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.
Veevas Vault Quality suite is a single authoritative source enabling greater visibility and control. Vault Quality enables organizations to modernize quality management assuring quality while driving compliance and operational innovation. We are looking for Consultants with Life Sciences experience and a passion for helping customers optimize their quality data and document management operations in the cloud.
What Youll Do
Participate in projects at life sciences companies designing and deploying Quality systems
Support Functional Analysts in workshops and be part of customer discussions of the Vault Quality suite (Vault QMS Vault QualityDocs Vault Training)
Quality/Content management solution design prototyping configuration and documentation
Solution and configuration of Veeva Vault Quality Suite per customer requirements including workflows document types security fields page layouts reports dashboards formatted output reports and notifications
Leveraging enablement of outofthebox or best practices configuration approach to solution strategy
Assessing the impact of change on the current configuration and working with key stakeholders to make informed decisions in a timely manner
Represent Professional Services across multiple engagements and workstreams (e.g. solution design and configuration data migration systems integration etc.
Ensure customer success from the beginning to the end of the engagement life cycle
Requirements
4 years of experience implementing Document or Quality Management systems for life sciences as a consultant business or IT representative
Bachelors Degree in Life science computer science or related degree
Solid analytical and great interpersonal skills
Excellent communication skills (written and verbal)
Strong attention to detail
Highly organized
Ability to act with speed to understand business requirements and willingness to roll up your sleeves to design and implement a solution
Exposure to life sciences compliance and computer systems validation requirements
Nice to Have
Understanding of global quality requirements compliance considerations and processes for Quality process and content management life sciences compliance and/or computer systems validation
Proven track record leading highimpact global system implementation programs as a consultant business or IT lead and/or business sponsor
Direct experience with systems such as Veeva Vault ETQ Reliance Sparta TrackWise OpenText SharePoint Documentum D2 FirstDoc
FirstPoint NextDocs UL ComplianceWire and other quality information management or content management systems
SaaS/Cloud experience
Knowledge of Quality operations within the Life Sciences Pharmaceutical Biotech industry and/or equivalent.
Perks & Benefits
Flexible PTO
Health & wellness programs
#LIRemote
Veevas headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color sex sexual orientation gender identity or expression religion national origin or ancestry age disability marital status pregnancy protected veteran status protected genetic information political affiliation or any other characteristics protected by local laws regulations or ordinances.
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