The Role
Looking for an opportunity to innovate? Interested in consulting? Come help us change how Quality information, content, and processes are managed in Life Sciences. Veeva Quality suite is a single authoritative source, enabling greater visibility and control. Veeva Quality enables organizations to modernize quality management, assuring quality while driving compliance and operational innovation.
We are looking for driven, self-motivated Consultants with Life Sciences experience and a passion for helping customers optimize their quality data and document management operations in the cloud.
As a key member of our China Professional Services team, you will work side-by-side with customers and our solution architects to implement Veeva Quality products. In this role, you will lead the overall delivery of Veeva Quality Suite for our customers. You will define and drive business processes, lead the project team in delivering the solution, and guide our customers throughout the implementation programs.
As a Consultant, you will actively collaborate across Veeva, contributing ideas, enhancing our delivery model, and working closely with our product management team to meet the evolving needs of the industry.
What You’ll Do
- Participate in projects at life sciences or biotech companies designing and deploying Quality systems
- Rapidly configure and implement the Veeva Quality suite (Veeva QMS, Veeva QualityDocs, Veeva Training, Station Manager, Validation Management, and LIMS)
- Lead requirements workshops: design, prototype, configure, and document content management and/or data solutions
- Project management including resource planning, leading and motivating a cross-functional team, and project tracking and forecasting
- Ensure customer success from beginning to end of the engagement life cycle
- Mentor project team and junior consultants
- Assist presales/sales teams in defining scope, cost, and estimations
Requirements
- Strong written and verbal communication skills in both Chinese and English
- Deep experience of Quality processes in Life Sciences and the relevant compliance considerations and/or understanding of the principles of Content Management
- Experience implementing Document or Quality Management systems for life sciences as a consultant or IT representative
- Knowledge of Quality operations within the Life Sciences, Pharmaceutical, Biotech, Medtech industry, and/or equivalent
- Understanding of Computer Systems Validation
- Ability to translate technology to the business or end-users
- Ability to act with speed to understand business requirements and a willingness to “roll up your sleeves” to design and implement a solution
- Exposure to life sciences compliance and computer systems validation requirements
- Demonstrated work history in stakeholder management, critical thinking skills, ability to conduct complex communications in a wide variety of settings and audiences
- Ability to travel 10-30% within China
- Candidate must be based in Shanghai/Suzhou and have the legal right to work
Nice to Have
- Understanding of Learning Management Systems and GxP training needs and regulations
- Understanding of LIMS
- Proven track record leading high-impact global system implementation programs as a consultant, business or IT lead, and/or business sponsor
- Direct experience with Quality Management, Learning Management, Content Management, and/or Laboratory Information Management systems (for example, Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, Compliance Wire, Cornerstone, LabVantage)
- Life science, computer science, or related degree
- SaaS/Cloud experience
- Experience in services delivery management and/or systems implementation
Perks & Benefits
- Fitness fees
- Veeva break