Key Responsibilities:
- 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
