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Job Details


Novartis

Quality Documentation Specialist (347539BR)

Pharmaceuticals

All

Yearly

No

Melville, New York, United States

Job Description With 64 manufacturing sites in 26 countries, our aspiration is to become the top manufacturer of innovative and generic medicines in the industry!

This role is essential to maintain proper management of QA documents with responsibilities such as BRFs Archive Room management (inventory, archiving, retrieving for APQRs and HA Inspections, disposing records past retention), eSOPs Index management/ quarterly reconciliation, and management of manual training records.

This role will also assume the responsibility of acting as the primary coordinator and administrator for Condor, U4G, Global Indexing tool and CIRF.

This position will ensure above responsibilities assigned to a dedicated associate with proper training and allocated time supporting the entire Fougera QA organization's effort to maintain proper compliance and data integrity