Office-III-AR&D, Medreich R&D Centre, Bangalore, Karnataka, India, 05/01/16, Present, Handling of Caliber LIMS Software, To follow STP, SOP's, GLP, cGMP and ICH guidelines., Creation of Product code, Specification ID in CALIBERLIMS., Creation of work sheet and Test in CALIBERLIMS., Creation of Test plan & TTDC in CALIBER LIMS., Creation of Stability Study Protocols, Condition Labels & Sample Storage., Review of documents in caliber LIMS., Stability Chambers, Maintaining of Stability Chambers., Documentation as per cGMP & GLP., Review of stability protocols., Stability samples charging & Withdrawal as per schedule., To follow safety health and Environment norms and adhere with company policy., To prepare stability summary report data as per schedule., Instruments Handling, Handling of HPLC Agilent 1100, waters e2695 with Empower3., Handling of Dissolution: Electro lab & lab-india auto sampler & manual USP Type I, II, III., UV: Shimadzu with UV probe., Major Regulatory Audits of WHO, ANVISA, US-FDA, MHRA, Other GMP and party audits., Customer Audits., Internal Audits from Plant QA and CQC Audits.