Deputy Manager - Manufacturing QMS

Key Responsibilities

JOB DESCRIPTION

• Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturing department
• Document preparation like CCF, SOP, Investigation, Risk Assessment, Protocol etc.
  
  

Skills

• 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

Qualification: M.Sc B.Pharm / M.Pharm

Experience : 8 - 11 years
Skills Required
Report Writing, Regulatory Compliance, capability development