09 Aug
|
SVR Drugs And Intermediates
|
Bengaluru
09 Aug
SVR Drugs And Intermediates
Bengaluru
Experienced QA skilled with 1012+ years in pharmaceutical bulk drug manufacturing. Responsible for cGMP compliance, QMS, deviations, CAPA, change control, OOS/OOT, SOP,BMR'S, audits, validation, regulatory compliance and quality documentation.
📌 Quality Assurance - Senior Executive (Bengaluru)
🏢 SVR Drugs And Intermediates
📍 Bengaluru