Ajinkya K Pawar

Accomplished Production Executive with a proven track record at Indoco Remedies Limited, recognized for outstanding performance during the USFDA Audit in 2023. Demonstrates exceptional analytical skills and a positive attitude, excelling in manufacturing operations and workflow optimization. Skilled in MS-Office and adept at fostering cross-functional team collaboration to exceed production targets.

• Executed batch activities in prominent audits, including USFDA, WHO, and various regulatory agencies while at Cipla.
• Received recognition from the department head at Cipla for presenting innovative ideas during specific activities.
• Successfully navigated customer audits and participated in major regulatory audits such as USFDA, TGA, and others during my tenure at Glenmark and Aculife.
• Acknowledged and awarded for outstanding performance during the USFDA Audit at Indoco in 2023.

Sterile Academy CIPLA (Aseptic Process Activity): Cleaning activity of critical processing area and Aseptic assembling, filling Activity modular training.

• Date of Birth: 21/03/94
• Nationality: Indian

• Hindi
• English
• Marathi

• Music
• Travelling

I, Mr. Ajinkya Kushaba Pawar, affirm that, the information compiled above is precise and accurate in its entirety to my knowledge.

Engaged in diverse sports activities and actively participated in social service initiatives during my college years.

• Incharge on production Injectable (Ampoule/Vial) Line 3 where supervised the production line, ensuring smooth and efficient operations.
• Collaborated with cross-functional teams to optimize workflow and meet production targets.
• Monitored and maintained equipment to enhance productivity and minimize downtime.
• Currently managing soft floor line operation related to Manpower handling and also Batch Processing (manufacturing, filling and Terminal sterilization) activities.
• Managed the installation, qualification, and requalification processes for equipment.
• Handled deviations, OOS incidents, as well as OOAL and OOAC.
• Oversaw change control procedures related to documents, equipment, and facility modifications.
• Ensured strict adherence to aseptic practices in the aseptic area during daily operations.
• Conducted in-process checks throughout batch manufacturing, filling, and vial inspection areas.
• Ensured the real-time online documentation of production activities in accordance with current Good Manufacturing Practices.
• Proficiently operated autoclaves from manufacturers such as Metalchem, Pharmalab, and Fedegeri.