Lead CSV & QV QA Specialist – Pharma Compliance

Dormont Manufacturing Co is launching a new production site in Bern, searching for a professional to oversee Computer System Validation (CSV) and Qualification processes. In this key role, you will ensure superior quality standards in pharmaceuticals, contributing to safe and effective product deliveries. Ideal candidates will possess at least 5 years of experience in CSV and profound knowledge of regulatory standards. Join us to make a lasting impact in a vibrant work environment.
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