Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Post : CT QA Auditor
Department : QA
Qualification : M.Sc, B.Pharma, M. Pharma Others
Experience : Min: 8 Year(s) - Max: 12 Year(s)
Primary Skills : • QMS
• Audit & Inspection Readiness
• Auditing
• Timeline Management
• CSV Validation and qualification
• Sponsor Handling
• Knowledge of regulatory guidelines and compliance requirements
Location : Cliantha Corporate
Brief JD : Auditing, QMS, CSV
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