12 Sep
|
Cadila Pharmaceuticals
|
India
12 Sep
Cadila Pharmaceuticals
India
Description
• To prepare and review the PQRs. • To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. • To verify & review of Ingredient manufacture name (Vendor Name) & TSE-BSE certificate for PQR Compilation. • Review for Qualification & validation data for compilation of PQR. • To perform continuous process verification of the product. • To initiate & review Change Control, Deviation & CAPA in LIMS. • Any other job assigned time to time by HOD as per requirement.
📌 Senior Executive (India)
🏢 Cadila Pharmaceuticals
📍 India