Executive Manufacturing QMS and compliance Injectable

Role Overview: - You will be responsible for the preparation and review of master documents for sterile manufacturing in the parenteral facility. - Your role will involve preparing and reviewing protocols and reports as per requirements. - You will handle document management and preparation of BMRs, BPRs, master SOPs, etc. - Managing change control, deviations, CAPA, investigations will also be part of your responsibilities. - Providing training to subordinates, technicians, and operators in the department will be your duty. - Ensuring audit and compliance on the manufacturing shop floor. - Utilizing knowledge of kaizen and continuous improvements. Key Responsibilities: - Prepare and review master documents for sterile manufacturing. - Create protocols and reports based on requirements. - Manage document preparation including BMRs, BPRs, master SOPs, etc. - Handle change control, deviations, CAPA, investigations. - Provide training to subordinates, technicians, and operators. - Ensure audit and compliance on the manufacturing shop floor. - Implement kaizen and continuous improvement practices. Qualification Required: - B.Pharm/M.Pharm candidate with a minimum of 3-5 years of experience in manufacturing QMS/Process review/Compliance.,