Quality Systems (Veeva) Senior Consultant
On-sitePhiladelphia, Pennsylvania, United States or Raleigh, North Carolina, United States
Philadelphia, Pennsylvania, United States or Raleigh, North Carolina, United StatesOn-siteFull TimeSenior LevelBachelors DegreeMedium
Full TimeSenior LevelBachelors DegreeMedium
Job Summary
Design and deploy Veeva Quality suite and Vault RIM capabilities for life sciences and consumer products clients. Lead requirements workshops, configure content management solutions, and oversee project plans while managing scope and resource allocation. Assist in GMP system validation, revise SOPs, and conduct end-user training to share best practices. Provide guidance to junior analysts and build trusted client relationships that extend beyond individual projects. This role requires 5+ years of life sciences experience, 30-50% travel, and a 4-year degree.
Required Qualifications
- 5+ years of experience working with or for life sciences companies
- Experience implementing Document or Quality Management systems for life sciences as a consultant, business, or IT representative
- Understanding of global quality requirements, compliance considerations, and processes
- Firsthand experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, or other quality information or content management systems
- Team Lead experience
- 4-year degree from an accredited college or university
- Travel is an integral part of this role and is estimated to average 30-50%
- Relocation is not required
Desired Qualifications
- Experience with regulatory information management systems, including registrations and submissions, preferred
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