15 - 18 years
20 - 25 Lacs
Posted:2 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities To review and maintain production schedule as per the project/priority and as per the availability of the required material & all other related resources. Responsible for production related activities of Block and timey execution of production planning batches/activities Optimum utilization of man, material and machinery oi pharmaceutical products To deal with outside parties for changes, improvements in equipment, process which direct impact on product quality. To review and approve documents through QMS software if applicable, but not to, SOP, Change Centre, Planned Modification, Event and investigate reverts. Monthly/Quarterly/Half yearly/yearly report Study protocol and report, Qualification report and protocol.Other relevant documents as applicable. To review the document like MF, BMR (Batch Manufacturing Record), BOM (Bill of Material). Preferred candidate profile : Should be from Injectables background with USFDA experience
Sun Pharma
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My Connections Sun Pharma
Baska,Gujarat
20.0 - 25.0 Lacs P.A.