Hiring "Training & SoP Author Lead - Regulatory" | 100% Remote (UK/EU)
London, United Kingdom
Hybrid / WFH Options
Hybrid / WFH Options
Smartedge Solutions Ltd
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 More ❯
Employment Type: Contract
Rate: GBP Annual
Posted: