Posted:1 week ago|
Platform:
Work from Office
Full Time
1. Review and understanding of product related technicalities for smooth transfer of products to Internal Manufacturing facility of Strides or External Facility.
2. Co-ordination and collection of technical documents from internal sites.
3. Review of Tech pack documents and sharing (MFR, MPR, Spec/STP, BMR, BPR, Tool drawings layouts etc.) to Internal or external manufacturing sites.
4. Review of Master documents before initiating validation batches at Internal or external manufacturing sites.
5. Conducting/Monitoring of Feasibility trials/ Scale up trials at R&D or Manufacturing site.
6. To be involved in cost improvement program for identified product, to change the formula and improvise the process as required.
7. Handling of Trouble shooting to improve the product quality attributes.
8. Ensure Test license availability at R&D & Plant.
9. Ensuring Tooling’s and RM’s availability for execution of lab trial batches, PO/PE/Scale up batches and monitoring the batches during execution.
10. Preparation and Review of Trial Reports.
11. Preparation and review of stability protocol for experimental batches.
12. Initiation of the test request for the analysis.
13. Process optimization activities for internal/external products as identified and assigned.
14. GMP, GDP, Quality Management systems and SOP shall be followed to ensure the continuous compliance.
Strides Pharma Science
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