-Deliver production as per supply plan, achieve the best achieved process efficiencies-Maintain the highest standards related to safety, health, environment and housekeeping-Improve process efficiencies and people productivity along with the plant team-Review and approve SOP, BMR, BCR, BPR, Change Controls, Incident reports, OOT & OOS reports, Validation Protocol, Validation Reports etc.-Monitor cGMP activities in plant with a view to keep the facility All Time Ready for regulatory and customer audits.-Maintain the plant with Integrated Pest Management principles.-Validated products with new equipments ANFD ,Co-Mill to enhance production capacity.-Handled qualification and Usage of DCS system in plant for automation of process in cGMP environment with total compliance 21CFR part11 standards.-Enhanced the capacity of plant through LSS principles.

-Handled the plant of 90KL volumetric capacity.-Meet the production targets with close monitoring of production activities.-Implemented 5s methodology in plant.-Handled the documents with ALCOA+ principles.

Worked for USFDA , KFDA, MHRA, WHO Approved facility , mfg. plant (2KL to 9KLreactors, with 96KL volume )with the responsibilities like -Execute the batches with respect to MBR and SOP'S . -Achive production targets without any OOS ,OOT,Deviations -Implementation of kizen and 5S.-Monitor and improve processes -Identify quality and productivity problems.-Ensuring compliance with GMP and Safety standards.-To handle process in equipment's like GLR,SSR,CF,SF,ANF.ANFD.MM.FBD.VTD.TD.RCVD.

-To maintain the cGMP enviornment in plant -To handle the production activities as per planning- Handled equipments used in API manufacturing such as SSR ,GLR ,CF,SF,TD,VTD,VS,OB,MM,JM.etc- worked in clean room Area- hands on experience for maintaining and handling various customer and authority audits.