Talentmate
India
19th August 2026
2608-6430-149
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.
| 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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