Deputy Manager - Manufacturing QMS

As a Supervisor in the Sterile manufacturing department, your role involves the preparation, review, revision, control, and implementation of standard operating procedures activities. You will also be responsible for overseeing Change control and CAPA processes. Your key responsibilities include: - Preparation, review, revision, control, and implementation of standard operating procedures activities - Oversight of Change control and CAPA processes - Document preparation such as CCF, SOP, Investigation, Risk Assessment, Protocol, etc. To excel in this role, you should possess the following qualifications and skills: - Quality Management Systems: Mastery level - CAPA (Corrective and Preventive Actions): Mastery level - Regulatory Compliance: Expert level - Change Control Management: Expert level - Report Writing: Expert level - Audit & Inspection Readiness (Internal & External Audits): Expert level - Capability Development: Expert level - Manufacturing Process and Equipment Understanding: Expert level - Communication & Collaboration: Expert level If there are any additional details about the company in the job description, kindly provide them for further insights.,