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5.0 - 10.0 years

5 - 10 Lacs

hyderabad, telangana, india

On-site

Responsible for Monitoring and support the Quality assurance of Vaccines under Development/Clinical/Technology Transfer To ensure the compliance of product manufacturing against pharmacopoeia, WHO and other applicable regulatory guidance documents. To monitor and ensure the shop floor compliance for manufacturing of clinical and Tech-Transfer batches. To monitor and ensure the compliance of cell bank management. Review of executed BPRs, testing reports, COA and EMP data for the development batches. Handling and follow up for timely closure of Change Controls, Deviations, OOS, Risk assessment and OOLs. Review & Approval of Protocols (PV,CV etc.), study reports, BPRs, MFRs SOPs and other docum...

Posted 1 month ago

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