Implementation Consultant - Regulatory Systems
Veeva Systems, China

Experience
1 Year
Salary
0 - 0
Job Type
Job Shift
Job Category
Traveling
No
Career Level
Telecommute
No
Qualification
As mentioned in job details
Total Vacancies
1 Job
Posted on
Mar 25, 2021
Last Date
Apr 25, 2021
Location(s)

Job Description

At Veeva, we build enterprise cloud technology that powers the biggest names in the pharmaceutical, biotech, consumer goods, chemical amp; cosmetics industries. Our customers make vaccines, life-saving medicines, and life-enhancing products that make a difference in everyday lives. Our technology has transformed these industries; enabling them to get critical products and services to market faster. Our core values, Do the Right Thing, Customer Success, Employee Success, and Speed, guide us as we make our customers more efficient and effective in everything they do.
The Role
You are a Consultant with either Life Sciences or IT implementation experience. You have a passion for helping customers optimize their regulatory data and content management operations in the cloud. As a key member of our Professional Services team, you will be responsible for: understanding our customer needs, managing regulatory information, translating requirements into solution design, and defining global strategies to deploy our cloud-based solution across the enterprise.
Come help us change how Regulatory information, content, and processes are managed in Life Sciences. Veeva’s Vault RIM Suite is a cloud-based solution enabling life sciences companies to improve visibility, data quality, and agility.What You’ll Do
  • Participate in projects at life sciences or biotech companies designing and deploying Vault RIM systems
  • Rapidly configure and implement the Vault RIM Suite (Vault Registrations, Vault Submissions, Vault Submissions Publishing, Vault Submissions Archive) which is used to manage regulatory processes and content in the cloud
  • Lead requirements workshops: design, prototype, configure, and document content management and/or data solutions
  • Ensure customer success from beginning to end of the engagement life cycle
Requirements
  • Strong written and verbal communication skills in both Chinese and English
  • 5+ years’ experience with minimum 3 years in either IT consulting / professional services environment or in life sciences QA, Clinical operations or Regulatory departments
  • Experience with content and/or data management systems with the ability to comprehend and translate business requirements and create corresponding solutions designs
  • 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 25-50% within China
  • CandidatemustbebasedinShanghai andhavethelegalrighttowork
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
  • Experience implementing Document or Quality Management systems for life sciences as a consultant, business or IT representative
  • Direct experience with systems such as Veeva Vault, Sparta TrackWise, OpenText, SharePoint, Documentum D2, UL ComplianceWire
  • Consulting experience
  • Life Science, computer science, bio chemical and mechanical engineers or related degree
  • SaaS/Cloud experience
Perks Benefits
  • Allocations for continuous learning amp; development
  • Fitness Reimbursements


Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Job Specification

Job Rewards and Benefits

Veeva Systems

Information Technology and Services - Berlin, Germany
© Copyright 2004-2024 Mustakbil.com All Right Reserved.