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 : (1-8 out of 8)
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
Competencies Excellent communication skills in English and Hindi Strong organizational and project management skills with the ability to multi task,prioritize,and manage operations. Education Qualific
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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