Company Overview
Role Purpose
Academic Stream
Work experience (in months)
Job Responsibility and key Decisions
Responsible for preparation, review and revision of the batch document s and SOPs.
Responsible for preparation of URS for new equipment and instruments.
Preparation of the Qualification protocols for the new equipment and Instruments.
Identification and raising of deviation, change controls and compiling other GMP documents.
Responsible for implementation and closing of the CAPA related to Facility equipment and process.
Responsible for taking initiation for improvement in the process and procedure.
Responsible for ensuring there shall no deviation of the standard Operating procedure during production.
Should be responsible for monitoring of the Production activity and output.
Should have Audit experience USFDA, MHRA, EMA etc.
Should have experience on Pen assembling, Packing and handling new projects.