Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices accuracy with the email build, Subscriber segmentation, Journey configurations, and deployment accuracies. Calls out and communicates all inconsistencies to Campaign Managers and Deployment teams.
Preparation of documents and facilitation of documentation management in R&D while following established guidelines for correctness, completeness and clarity.
The role is responsible to asses / audit Sun manufacturing sites against current regulatory expectations / standards to ensure regulatory compliance. It includes adhering to applicable regulations, as well as Sun Pharma's policies and procedures.
Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical method development and validation for pharmaceutical dosage forms.
Responsible for In-process production related activities in DP manufacturing, filling, and packing sections. Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records.
Any M.Pharmacy / MSc (Full time) with 6 to 10 Years (or) B.Pharmacy with 8 to 12 Years of relevant Experience in Manufacturing (Upstream/Downstream) injectables with Strong people management
This candidate will primarily work a shift-based schedule to enable the business in delivering Amgens mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs.