Experience

Baroque Pharmaceuticals Private Limited

• India
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Deputy Manager QA

  • Mar 2019 - Jul 2021

  Taking care of penicillin facilities, overall responsibilities of IPQA, Documentation, QMS,training, customer support, Audit observations and compliance management, Validation, Project management, Taking care of penicillin facilities, overall responsibilities of IPQA, Documentation, QMS,training, customer support, Audit observations and compliance management, Validation, Project management,



Bharat Parenterals Ltd

• India
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Assistant manger QA

  • Dec 2017 - Mar 2019



Baroque Pharmaceuticals Private Limited

• India
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Assistant Manager QA

  • Dec 2015 - Dec 2017



Medley Pharmaceuticals Ltd

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Asst- Manager QA

  • Mar 2011 - Dec 2015

  Previously worked with medley as key responsible person looking Responsible for IPQA entire Production activity,Responsible for co-ordination with all departments,Responsible Release of finished goods for marketing distribution,Responsible review and approval of COA,COC for finished product,Responsible review of annual product quality review,To ensure continuous system improvement by reviewing documents and carries out self audits of various departments in plant. Responsible review and… Show more Previously worked with medley as key responsible person looking Responsible for IPQA entire Production activity,Responsible for co-ordination with all departments,Responsible Release of finished goods for marketing distribution,Responsible review and approval of COA,COC for finished product,Responsible review of annual product quality review,To ensure continuous system improvement by reviewing documents and carries out self audits of various departments in plant. Responsible review and approval of SOP’s Master MMD’s, MPD’s. BMR’s, BPR’s, Protocols and other master documents,Responsible for review of Process Validation Protocol/Report and Monitor entire activity. Faced and contributed in Successful completion of MHRA-UK (Jan 2014) and other ROW Audits Show less Previously worked with medley as key responsible person looking Responsible for IPQA entire Production activity,Responsible for co-ordination with all departments,Responsible Release of finished goods for marketing distribution,Responsible review and approval of COA,COC for finished product,Responsible review of annual product quality review,To ensure continuous system improvement by reviewing documents and carries out self audits of various departments in plant. Responsible review and… Show more Previously worked with medley as key responsible person looking Responsible for IPQA entire Production activity,Responsible for co-ordination with all departments,Responsible Release of finished goods for marketing distribution,Responsible review and approval of COA,COC for finished product,Responsible review of annual product quality review,To ensure continuous system improvement by reviewing documents and carries out self audits of various departments in plant. Responsible review and approval of SOP’s Master MMD’s, MPD’s. BMR’s, BPR’s, Protocols and other master documents,Responsible for review of Process Validation Protocol/Report and Monitor entire activity. Faced and contributed in Successful completion of MHRA-UK (Jan 2014) and other ROW Audits Show less