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.
WALK-IN INTERVIEW Bioanalytical
MDMV / Sample Analysis
Qualification : M.Sc., B.Pharm, M.Pharm
Experience : 4-10 years
• Person should have appropriate knowledge of sample extraction and able to perform the sample processing activities.
• Knowledge of operations of Sciex mass spectrometer instrument is desirable, regulatory knowledge of method validation guidance is must.
• Operational knowledge of analytical instruments is required.
Report Writer
Qualification : M.Sc., B.Pharm, M.Pharm
Experience : 1-4 years
• Person should have knowledge of regulatory (USFDA, EMA, ANVISA, etc.) requirements.
• Responsible for the preparation of bioanalytical report and method validation report.
• Handle sponsor and regulatory queries on report.
Eligibility : Experienced candidates only.
Walk in Interview
Date : 27th May 2023 (Saturday)
Time : 2:00 PM to 05:00 PM
Location : 3rd Floor, Commerce House II, Opp. Pushparaj Towers, Judeges Bungalow Road, Bodakdev, Ahmedabad 380054
Share your CV at srchauhan1@cliantha.com or recruitment1@cliantha.com
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