Veeva Consultant

As a Senior Consultant Pharmaceutical QMS GxP, you will be responsible for leading the design and implementation of Quality Management Systems (QMS) in GxP regulated pharmaceutical environments. Your role will involve combining deep expertise in business analysis and eQMS implementation with strong advisory capabilities in process harmonization and regulatory compliance. You will play a pivotal role in delivering scalable compliant QMS solutions as a key member of the Life Sciences R&D consulting team. Your responsibilities will include: - Leading workshops to assess current QMS maturity and define future state processes - Designing scalable GxP compliant QMS frameworks tailored to client needs - Collaborating with cross-functional teams to gather and document requirements across functional migration and integration workstreams - Translating business needs into functional specifications using tools like JIRA and HP ALM - Implementing and supporting supplier qualification audits, performance monitoring, and risk management processes - Integrating supplier quality workflows into enterprise QMS platforms In terms of technical requirements, you should have proven experience in eQMS design and implementation within GxP regulated environments. Additionally, you should possess in-depth knowledge of QMS processes such as supplier quality audit processes, risk management, change control, deviation, complaints, etc. Hands-on experience with leading QMS tools such as Veeva Vault, TrackWise, TrackWise Digital, ETQ Reliance, and MasterControl is essential. A strong background in business analysis, stakeholder engagement, and regulatory compliance is required, along with excellent communication, facilitation, and project management skills. You should be able to work both independently and collaboratively across global teams. While a degree in a technical, scientific, or clinical discipline is preferred, the preferred skillset includes expertise in Veeva Vault, specifically in the context of Life Sciences, CTMS/Trial conduct.,