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CLIANTHA RESERACH WALK IN INTERVIEW FOR B. PHARM / M. PHARM / MSC CANDIDATES IN QUALITY CONTROL & QUALITY ASSURANCE DEPARTMENTS.

 CLIANTHA RESERACH WALK IN INTERVIEW FOR B. PHARM / M. PHARM / MSC CANDIDATES IN QUALITY CONTROL & QUALITY ASSURANCE DEPARTMENTS.

ABOUT CLIANTHA RESERACH:

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.

JOB DETAILS:

Cliantha Research Limited looking for dynamic individuals  B.Pharm/ M.Pharm/ M.Sc candidates for the position of Officer/ Sr. Officer in Quality Assurance & Quality Control departments to join our growing team. Interested and eligible candidates can attend Walk-in interviews on 12th February 2022 Saturday, at 10 am


DEPARTMENT: QA/ QC (BA Lab/

POSITION: Officer/ Sr. Officer

QUALIFICATION: B.Pharm/ M.Pharm/ M.Sc

EXPERIENCE: 2 to 6years.

JOB DESCRIPTION:

For QA/QC (BALab) JD: 

Review of data and reports related to the sample analysis.pharmacokinetic & statistical analysis reports and bioanalytical method validation reports. To conduct inprocess audits for study as well as method validation. 

Review of calibration | validation documents and CoAs of working/reference standards. 

Preparation and|orreview of SOPs. 

Conduct system audits in relevant departments and conduct vendor audit. 

Maintain master documents, calibration certificate and_ validation document related to laboratory. 

Ensure training of all applicable personnel involved during study activities. 

Ensure implementation of CAPAresponses. 

Issuance and archival of documents. 


For QA/QC(Clinic) JD: 

Online monitoring of studies to ensure that studies are conducted in accordance with GCP, SOPs, Protocol and regulatory guidelines. 

Review 100% of clinical raw data for completeness, accuracy. and for compliance with the Study Protocol, GCP, SOPs and applicable Regulatory Guidelines. 

Review of tabular listing appended to report and scan check of individual subject CRF as per clinical raw data, sponsor and regulatory requirements. 

Issuance, reconciliation and accountability of forms. 

Preparation of projects for QA audit and Archiving. 

Review of applicable SOPS.

WALK IN INTERVIEW:

INTERVIEW DATE : 12th February 2022 (Saturday)

TIME: 10:00 AM to 1:00 PM

VENUE : TP 86, FP 28/1, Off S. P. Ring Road, Opp. Apple Woods, Nr. Lakshya International School, Sarkhej, Ahmedabad – 382210.

For more details please contact at 

+91 6351946108, azode@cliantha.com.




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