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.
Cliantha Research — Walk-In Interview QA / QC Team
QA Auditor
• Conduct in-process and retrospective audits for studies and method validations.
• Review reports, source data, audit trails and regulatory compliance.
• Audit study protocols, SAPs, deviations, change controls and QMS documents.
• Review calibration, validation, sample shipment and temperature-monitoring records.
• Support system audits, vendor audits, regulatory inspections and query management.
QC Reviewer
• Review bioanalytical and large-molecule study data for accuracy and compliance.
• Verify study protocols, SOP adherence and regulatory requirements.
• Prepare and review calibration, QC and concentration data tables.
• Ensure timely data review, release and archiving of study documents.
• Support audit readiness, documentation control and project tracking.
Experience : 0–5 Years
Qualification : B.Pharm / M.Pharm / M.Sc
Walk-In Details
Date : Saturday, 12th September 2026
Time : 10:00 AM – 2:00 PM
Venue : Cliantha Research Ltd.
Cliantha Corporate, TP 86, FP 28/1,
Off S.P. Ring Road, Sarkhej,
Ahmedabad, Gujarat – 382210
Documents to Carry
• Updated resume
• Two passport-size photographs
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