. To prepare Master documents of Analytical Method Development / Analytical reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP of MIC creati
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Excellent organizational and time management skills. Bachelors degree in Education,. Experience in a similar role within the pharmaceutical industry is a plus. How to Apply: .
Knowledge of scale-up processes,and familiarity with Good Manufacturing Practices (GMP) and ICH-guideline. . Hands-on experience with bench-scale and pilot-scale synthesis is essential. Preferred ca
To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP. . MIC creation o
To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP. . MIC creation o
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