Quality Analyst I

3.00 to 6.00 Years Bangalore 29 Sep, 2020

Job Location	Bangalore
Education	Not Mentioned
Salary	Not Disclosed
Industry	Pharma / Biotech
Functional Area	General / Other Software
EmploymentType	Full-time

Job Description

To ensure compliance to good clinical practices, good data management practices, standard operating procedures, protocols, regulatory requirements and applicable principles of good laboratory practices in clinical development, investigators sites and documentation of any deviations from the above.
Check for compliance of study related activities to good clinical practice, concerned standard operating procedures and protocol.
Review the protocol and case report form.
Conducting site audit, facility and quality system audits
Review of edit check plan and edit check software program (User acceptance testing).
Review the validated clinical trial data to ensure consistency, integrity and accuracy based on project specific requirement.

Qualifications

M.Sc/ m.Pharm/ Graduate in lifescience

Function Quality Sub Function RD Quality ,

Keyskills :
qualitycustomer relationstest casescalibrationauditinguser acceptance testinggood clinical practicestandard operating proceduressystem auditquality systemdata managementuser acceptancemanagement auditacceptance testingclinical practicesclin

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Quality Analyst I

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