Mayur Chhajed

To pursue a growth oriented career with a progressive company that provides a scope to apply my skills and professional experience that would help me to contribute my best to the organization.

USFDA, TGA, UGANDA, KENYA, MHRA, and WHO etc.

• All IPQA activities and QMS activities.
• Performing In-process Quality checks for Tablet manufacturing and packaging.
• Responsible for line clearance for dispensing, granulation, compression, coating and packing areas.
• Responsible for batch release.
• Execution and monitoring of process validation activity.
• Review of Batch records and analytical reports of batches.
• To operate SAP system based on roles and rights provided in the application.
• Responsible for investigation of queries received from Regulatory agencies related to registration as well as commercial products.
• Responsible for routine inspection of various departments to maintain cGMP compliances at all levels.
• Continuous vigilance to ensure conformance to SOPs, instructions and prevention of risk throughout the plant to avoid mix-ups and cross contamination.