2 - 6 years

0 Lacs

Posted:1 week ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

You will be responsible for the issuance, control, and retrieval of documents. Your duties will also include scanning and uploading approved paper-based documents in Veeva Vault, as well as maintaining master copies for SOPs. Additionally, you will be involved in conducting and organizing training sessions, maintaining Vendor audit and Technical agreement planners, and preparing/reviewing SOPs, Protocols, and other cGMP documents. You will also be tasked with tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with stakeholders for timely closure. Location: Ferring India Laboratories,

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Ferring Pharmaceuticals logo
Ferring Pharmaceuticals

Pharmaceutical Manufacturing

St-Prex

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