Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
All Jobs : (1-5 out of 5)
. 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
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
Preferred candidate profile . M Sc in Chemistry/ M Pharm/ PhD in PharmacyExperience . 15-20 years of experience (~3 years in senior leadership
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