Job Description

Job description: Core responsibility related to GLP: Receipt of request for controlled/uncontrolled documents Issuance of controlled/uncontrolled documents Archival, retrieval/re-archival of documents Maintain study plan, SOPs and other documents at RQA as per SOPs Co-ordinate the RQA and other test facility personnel for day-to-day activities Update the RQA records as and when required in compliance with SOPs. Allied responsibility: Review of efficacy-Non-GLP study raw data and study reports and issue the inspection report. Report the inspection/audit finding to the study scientist and management. Any additional responsibilities/activities as and when assigned by management which would not arise conflict of interest.


Job Details

Role Level: Entry-Level Work Type: Full-Time
Country: India City: Dholka ,Madhya Pradesh
Company Website: https://www.cadilapharma.com/ Job Function: Others
Company Industry/
Sector:
Pharmaceutical Manufacturing

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