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
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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
Knowledge of regulatory expectations for APIs and CMC documentation preferredExperience: . 1 to 3 years (Research Associate Entry level) . Strong hands-on experience in peptide API process developme
Ideal Candidate Profile: . 6-10 years of relevant experience in pharma project managementExperience in tech transfer will be an added advantage
. 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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