QMS Lead

About the role

Responsible for preparation, review, revision, control and implementation of standard operating procedures of sterile manufacturing department & warehouse department. Responsible for preparation & review of the master documents of sterile manufacturing department and warehouse department for Parenteral facility -I, II & III.

What you'll do

• Responsible for preparation, review, revision, control and implementation of standard operating procedures of sterile manufacturing department & warehouse department
• Responsible for preparation & review of the master documents of sterile manufacturing department and warehouse department for Parenteral facility -I, II & III
• Responsible for preparation and review of Protocols and reports based on the requirements
• Responsible for Document management like BMR’s, BPR’s, Master SOP’s etc
• Responsible for the handling (Preparation/Initiation/Execution and Approval) of Change Control, Deviations, CAPA, Investigation, QRM, Protocol

What you need

• ISO 9001
• Learning and development
• Performance management
• Employee relations
• Recruitment
• SOP writing
• Any graduate

Good to have

• GMP