1. Comply with all applicable SOPs, GMP and safety regulations.
2. Review of Form 29 & License Documentation for getting manufacturing license and Form 29
3. Review and Finalization of Text Matter of Art Works of all dosage forms.
4. Review and Checking of Document of Master Formula Record of all doses form like- Tablets, Ointment, Cream, Sachet, Capsules, DPI, Blended pellets, Liquid Formulation-Oral spray, Nasal spray and so on) & their entry record.
5. Preparation and reviewing of Product Development Report.
6. Technology Transfer from R&D; to Commercial Batch.
7. Review and Approval of R&D; SOPs by following QA SOP on SOP.
8. Training of GMP & R&D; SOP.
9. Review of Stability Data of Recent Products.
10. Review of Target Specification of product.
11. Review Document of Product Development Report of all doses form like- Tablets, Ointment, Cream, Sachet, Capsules, DPI, Blended pellets, Liquid Formulation- Nasal spray, Topical solution) & their entry record.
12. Perform other related duties as assigned to meet departmental and company objectives.
📌 Formulation And Development Manager (Nalagarh)
🏢 Biodeal Pharmaceuticals
📍 Nalagarh
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