Job Description
- Develop and put in place effective quality assurance processes that meet regulatory standards.
- Create and maintain company quality policies Standard Operating Procedures (SOPs) and quality systems.
- Carry out internal audits and supplier/vendor audits as per cGMP ICH guidelines and other regulatory requirements.
- Monitor and review Corrective and Preventive Actions (CAPAs) and check if they are working properly.
- Check and review the quality of products regularly.
- Go through customer feedback and complaints to identify areas for improvement.
- Review failure investigations market complaints and OOS/OOT cases by working with the manufacturing technical and other teams to find the root cause and fix issues to prevent them from happening again.
- Prepare and share quality assurance reports with management.
- Make sure warehouse operations follow quality guidelines.
- Work with different teams to ensure everyone is following the same quality practices.
Job Type: Fulltime
Requirements
Qualification: M. pharm
Quality Management Systems (QMS) Internal & External Auditing Regulatory Compliance Root Cause Analysis & CAPA Document Control: Process Improvement