Deputy Manager - Manufacturing QMS

The Supervisor role involves the preparation, review, revision, control, and implementation of standard operating procedures, Change Control, and Corrective and Preventive Actions (CAPA) within the Sterile manufacturing department. You will be responsible for activities related to document preparation such as CCF, SOP, Investigation, Risk Assessment, and Protocol. Key Responsibilities: - Oversee the preparation, review, revision, control, and implementation of standard operating procedures, Change Control, and CAPA within the Sterile manufacturing department. - Manage document preparation including CCF, SOP, Investigation, Risk Assessment, and Protocol. Skills Required: - Quality Management Systems: Mastery - CAPA (Corrective and Preventive Actions): Mastery - Regulatory Compliance: Expert - Change Control Management: Expert - Report Writing: Expert - Audit & Inspection Readiness (Internal & External Audits): Expert - Capability Development: Expert - Manufacturing Process and Equipment Understanding: Expert - Communication & Collaboration: Expert Qualifications: - M.Sc B.Pharm / M.Pharm Experience: - 8 - 11 years In this role, your expertise in Quality Management Systems, CAPA, Regulatory Compliance, Change Control Management, Report Writing, Audit & Inspection Readiness, Capability Development, Manufacturing Process and Equipment Understanding, and Communication & Collaboration will be essential. Your experience of 8-11 years will be valuable in successfully executing the responsibilities of this position.,