Experience: Bachelor''s or Master''s degree in Pharmaceutical, Computer Science, IT, Engineering, or a related field. 10+ years of experience in Computer System Validation (CSV) in the pharmaceutical, biotech, or medical device industry. Strong knowledge of GxP, 21 CFR Part 11, GAMP 5, Data Integrity, and Annex 11. Experience in validating SaaS applications used in the pharmaceutical industry. Familiarity with Veeva Vault RIMS, QualityDocs, or Submissions Archive is a plus. Excellent documentation skills and experience with validation life cycle documentation. Ability to work independently and collaborate with cross-functional teams.