November 2003 — Present
High experience working in GMP environment,day to day operation in Tableting,Coating,Packaging environments,on shift cycle.Work on continuous improvement projects in Production,Participate in Fda/Imb audits.Following Sop's.Work as part of a team environment.Adhere to OEE targets for cycle times and changeover times.
Carry out in process testing during processing.
Validation of equipment prior to production processing.
Take Qc samples during in process tests.
Analyse any deviations and be willing to notify Supervisor/ Team lead.
Fill in Qc documents and carry out necessary corrections as per Sop.
Adhere to all Health and safety regulations.
Carry out cleaning of rooms and equipments as per Sop's.
Training of new Hires and existing employees,and perform in continuous improvement projects,5 s etc.