Bachelor’s degree or Master in Life Sciences, Pharmacy, Computer Science, or Related Domain.

4-8 years of experience in testing/verification of health, with at least 2-4 years in safety/medicine systems.

A strong understanding of drug safety (cases treatment, meddra/who drug coding, signal detection, rapid and periodic reporting).

Cooperation with the pharmaceutical and organizational safety and information teams and information technology teams to understand business requirements and compliance.

Practical experience with safety applications (for example, Oracle Argus, Arisg, Veva Safety, or the like).

Prepare a UAT strategy, test plans, test situations, and the tracking matrix compatible with URS (user requirements specifications).

Carrying out the UAT test programs, registry results, registry defects, and accuracy of tracking with sellers/sellers.

Checking the validity of the workflow related to cases of cases, sorting, medical review, reports, E2B (R2/R3), and discovering the signal.

Do the slope test for the safety, spot and integration system with safety/ medicines (Argus, ARISG, VAULT safety, etc.).

Ensure compliance with 21 CFR Part 11, GAMP 5 and GDPR and global drug requirements.

Support for final user training, preparation checks, and post -UAT signature.

Disclosure deviations, managing defect sorting calls, and ensuring time closure.

Prepare UAT Summary reports and contribute to the issuance of preparation assessments.

Supporting audit and inspection by providing UAT evidence and documents.

Contribute to the continuous improvement of UAT and test automation when necessary.