Inventia Healthcare is a pioneer in pharmaceutical development and manufacturing, with over 40 years of expertise in Oral Solid Dosage (OSD) forms. Our global presence spans 45 countries with over ten international facility approvals. Backed by Platinum Equity, we continue to innovate and grow with a solid R&D; base in Thane and manufacturing in Ambernath.
Location: Ambernath
Experience : 7 to 10yrs
Qualification: B.Pharm/M.Pharm
Working Days : 6 days
Reporting to: Lead Manager - QA
- To co-ordinate with BSR, Production and QC with respect to necessary documentation for batch release.
- Review of executed BMR, BPR.
- To review certificate of analysis, In-process analytical data, Process Analytical Data, Process Validation documents,
Annual Product Review documents.
- Approval of issuance BMR and BPR through Document Management System.
- To handle QCS inspection for Nigeria Products to get CIRA Report (Clean Report of Inspection and Analysis).
- Retention sample periodic review and destruction.
- Sample management for Regulatory dept., Marketing department. and Clients as per requirement.
- To provide reports to client and revert on queries.
- To ensure compliance of batch related documents and provide to regulatory department for submission.
- MES related activities-electronic batch record-preparation, review, and release activity.