Posted 8 Oct 2026 (28 days ago) · Job 18894 · Read from the employer's Lever board, last checked 5 Nov 2026, 19:09 UTC

Consultant - RIM Implementation

Veeva · China - Shanghai, China

Apply on Veeva’s site Ask about this jobApply opens the employer’s own application. Nothing is sent from here.

What the posting says

Each fact carries its state:Statedfound in the postingConflictstwo statements disagree, both quotedNot mentionedthe posting does not say

Employment typeStated: Full time
Work arrangementStated: On-site
Visa sponsorshipStated: no

Not mentioned in this posting

“Not mentioned” means the posting does not say. It is not a no. You could ask the recruiter.

PayNot mentioned: The posting does not say
ShiftNot mentioned: The posting does not say
ExperienceNot mentioned: The posting does not say
EducationNot mentioned: The posting does not say

Requirements, each with its sentence from the posting

These are the employer’s words. The index does not judge whether you meet them.

No requirement has been itemised for this posting yet. The employer’s words are in the full posting below.

Read the full posting as the employer wrote it

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Veeva is looking for individual leaders with consulting and system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.

Veeva’s RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform.

As a member of our Professional Services team, you will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and configuring our cloud-based solution for managing regulatory information across the enterprise.

What You’ll Do

Guide life science customers in the configuration and implementation of Veeva's Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes

Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions

Program and project management, including resource planning, leading and motivating a cross-functional team

Communicate between the project team, customer, and internal stakeholders

Assist presales/sales teams in defining scope, cost and estimations.

Requirements

Deep experience of Regulatory processes in Life Sciences and the relevant compliance considerations

3+ years’ experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative

Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution

Ability to collaborate and communicate excellently with diverse stakeholders

Team player with strong organization skills and an ability to act with speed in a complex environment

Strong written and verbal communication skills in both Chinese and English

Candidate must be based in Shanghai/Suzhou and have the legal right to work

Ability to travel 10-30% within China

Nice to Have

Consulting experience, working with a major system integrator or software vendor

Experience in life sciences compliance and computer systems validation requirements

#LI-Associate

Veeva’s 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.

The posting text is reproduced as the employer wrote it; the index adds nothing to it.

Apply on Veeva’s site Ask about this job