> Markdown version of [/jobs/ext/3944047-implementation-consultant-rim](https://www.wearedevelopers.com/jobs/ext/3944047-implementation-consultant-rim). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md).

---

# Implementation Consultant Rim

- **Company:** Veeva's Headquarters
- **Location:** Málaga, Spain (Remote available)
- **Contract:** Permanent contract
- **Skills:** Document Management Systems, Information Management, Software Engineering, Information Technology, Veeva
- **Published:** October 27, 2026
- **Apply:** https://www.adzuna.es/details/5942879625

## About the Role

3+ years in technology implementation services, in life sciences or healthcare
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 work hard in a fast-paced environment
Ability to travel as required by the business
Nice to Have
Consulting experience, working with a major system integrator or software vendor
Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
Experience in life sciences compliance and computer systems validation requirements
Fluency in one or more of the following languages: English, German, French, Spanish, Italian

## Description

Veeva Systems 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 Vault 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.
There is no work location requirement (remote position) within the EU/UK if a candidate is in close proximity to an airport and able to meet travel requirements. Qualified EU/UK-based candidates are encouraged to apply.
What You'll Do
Implement software and design solutions with our Veeva Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Submissions Publishing) at life sciences customers
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, Within 3 days, you will receive a link to a personality assessment administered by a third party.
Once you complete the assessment, our team will review your full application package and follow up via email with our decision.
If moving to the interview stage, the process is as follows:
A conversation with the hiring manager
A practical case exercise
A final conversation with our group's Senior Leader.
Once all interviews are complete, the manager will be in touch with a final decision.