(Summary generated by AI based on the full job description)
The project targets the pharmaceutical domain focused on Veeva Vault and Regulated Information Management (RIM). Requires at least 4 years in system analysis or consulting within pharma and solid knowledge of GxP in regulated environments. Responsibilities include managing configuration and validation documentation for RIM changes, conducting impact assessments and change analysis, gathering requirements and designing scalable solutions, overseeing implementation and validation, collaborating with Digital QA and Digital Enablement, and assessing Veeva release impacts. Preferred qualifications include Veeva Certified Administrator and experience with Jira Xray. Offered benefits include private healthcare, benefits cafeteria, car discounts, development support and profit-sharing.

Optional



By clicking "Aplikuj" you confirm that you've read and accepted our Terms and Conditions.
Certain terms used in this advertisement result from the standard layout and functionality of the website. They are technical in n ...
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Need more information?