4 - 8 years
5 - 8 Lacs
Posted:4 weeks ago|
Platform:
Work from Office
Full Time
1. Documentation related activities for Site Transfer Projects:- a. Teck pack evaluation for external site transfer projects and creation and approval of Techpack Index. b. Freezing of item codes for site transfer projects. c. Item code creation and approval - Raw materials and Semi Finished Goods (SFG) code creation and Creation of Finished Goods (FG) code for Exhibit batch for specific manufacturing location d. Preparation of stability protocols for Site transfer project of specific manufacturing location. e. Purchase Requisition (PR) initiation for Trial, PO, EB and VB batches and service PR for PDE and OEL reports.. 2.Drafting/Review and approval of Master Formula Records (MFR’s) for Site transfer projects 3. Revision / Review / Approval of Commercial Site transfer MFR’s (Including AVD code inclusion) 4. Drafting / Review / Approval of MES MFR’s and Handling of application interface of SAP and PLM 5. Handling of MQC/MIC updation and review. 6. Initiation, review & approval of Change Orders for updation of material master specifically for Site transfer codes. 7. Handling the SOP revision. 8. Approval of Artworks in OAMS related to first commercial batches of site transfer projects. 9. Impact assessment of CC related to site transfer projects, Initiation of CC for updation of MFR.
Strides Pharma Science
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