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.
📌 Apprentice (India)
🏢 Cadila Pharmaceuticals
📍 India
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