Qvents

Qvents

Discussion forum for Pharma Quality events, Regulatory Actions

Warning letters, 483s, Recalls, Import Alerts, Audit observations

Team Member QC

Analysis and Release of  Raw Materials ,Packing materials, Finished Products

Fill Finish Expert – Injectables

Responsible for Injectable Formulation Production activities.

Manufacturing QA Specialist

Perform In-process Process QA activities, the environmental monitoring of facilities and Utility systems, Audits and

QC Team Leader

Schedules laboratory analysis for a QC team, within a large QC department, Support the QC Team

Senior Officer – MSTG

Technology Transfer, Scale up and execution of exhibit batches, coordination with different departments

Global Quality Lead

Assure individual compliance with all concerned regulatory requirements, GxP’s and applicable department programs, including training,

Senior Research Scientist, AR&D

Analytical method development, validation for new products, comprehensive testing of API and finished dosages, Review

Executive QA

IPQA activities, Warehouse QA activities, MMaR’ S / MPaR’s Review.

Research Scientist – Stability Lab

Under guidance of Supervisor or senior chemist, responsible for performing all activities in ARD-Test Centre

Officer – Packing OSD

Packaging operations Oral Solid dosage forms, Labelling, Monitoring