Oversee preparation,review,and alignment of technical documents including PDRs,AMVs,validation protocols,batch records,and regulatory filing modulesMinimum Education Requirement . Masters degree in Ph
All Jobs : (1-9 out of 9)
Recommend and coordinate external development and manufacturing partners (CMO / CDMO) where requiredMinimum Education Requirement Educational and Experience Requirements . Utilize portfolio experience
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
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
. 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
Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
Graduate in any discipline .Experience of having worked any Trading / Pharmaceutical / FMCG CompanyThose who have worked in similar capacity in a Depot,Branch,CFA ( preferably) Distributor of FMCG,PHA
Graduateany stream),Preferably B.com Must have good knowledge of the modules of MS Office and should have worked on ERP Package like SAP / TallyPreference to those who have worked in a Branch/ Depot o
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