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
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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
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
Qualifications: . BE / B Tech or ME / M Tech in Chemical Engineering Professional certification in process engineering or related areasProficiency in process analysis,process modelling and simulation
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
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