Candidates only from Pharma company would be given preference Should have minimum of 2+ years experience in Pharma companyMust be proactive,self-driven,and energeticMust be a quick thinker,Extrovert,t
All Jobs : (1-7 out of 7)
Preference: Candidate must be from Pharma Industry Must be proactive,self-driven and energetic Must be a quick thinker,Extrovert,team player,enthusiastic,active listener,learning attitude Qualificatio
. 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
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
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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