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5.0 - 10.0 years

6 - 11 Lacs

hyderabad

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Experience: 5 to 10 years in QA . Qualification M Pharm or B.Pharm Review and approve development protocols , reports , and technical documents for formulation, analytical, and process development. Ensure development studies are conducted as per Good Documentation Practices (GDP) and QMS procedures . Oversee batch manufacturing records (BMR/BPR) and analytical data for R&D and scale-up batches. Participate in formulation and analytical strategy meetings to ensure quality alignment. Development SOPs and related quality documents. Master formula records and batch manufacturing records. Analytical method validation and verification protocols. Evaluate and assess changes raised during developmen...

Posted 4 days ago

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