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Cliantha Research Limited; Walk-In for M.Sc / B.Pharm / M.Pharm on 27th May’ 2023

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Cliantha Research Limited going to conduct a Walk-In interview for M.Sc / B.Pharm / M.Pharm on 27th May 2023 for the Ahmedabad location.

Cliantha Research Limited; Walk-In for M.Sc / B.Pharm / M.Pharm on 27th May’ 2023

About Company:

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission 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 is headquartered in India with facilities in Ahmedabad, Noida, and Vadodara.

We are conducting walk-in interviews for the following..!!!

PositionReport Viewer & Report Specialist
QualificationM.Sc / B.Pharm / M.Pharm
Experience1 to 6 yrs
No.of Openings:02

Time and Venue: 27 May, 2.00 PM – 5.00 PM
3rd Floor, Commerce House II, Opp. Pushparaj Tower, Judges Bungalows Road, Bodakdev, Ahmedabad – 380054, INDIA

Job description: Report Specialist:

Roles and Responsibilities:-

  • Prepare Sample analysis report and Method validation report in compliance with the standard operating procedure.
  • Ensure the report is prepared as per respective regulatory and sponsor requirements.
  • Handle Sponsors or regulatory queries on lab reports.
  • To ensure that lab reports are released within their timelines.
  • Maintain documents and databases for the assigned projects.
  • Compile copies of the Method validation report and Sample analysis report for archiving.

Report Viewer

Roles and Responsibilities:-

  • Ensure that the data is entered in a timely fashion to meet deadlines.
  • To ensure 100% validation data review for the completeness of documentation and compliance with all applicable standard operating procedures and regulations.
  • Ensure quality and integrity of data.
  • Maintain documents and databases for the assigned projects.
  • Ensure the completeness of documentation pertaining to method validation.
  • Report to the Study Director/R&D supervisor for method validation related to any deviations.
  • Review of Analytical Laboratory System for GLP Compliances.
  • Compile method validation for archiving.
  • Ensure reconciliation of forms after completion of method validation.
  • Preparation of summary tables of Method validation.
  • To assist the Project manager/Analyst in the preparation of the Analytical procedure.
  • Responsible for all activities of the Lab archivist in the absence of the Lab Archivist or as and when required.

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