Knowledge of about Preparation of SOPs and guideline. Knowledge of about Change control management. Handling of incidents, Deviations,Out of specification and OOT. Exposure to regulatory audits. Experience in conducting internal audits and audit preparedness. Implementation of good documentation practices. Knowledge about GLP and GMP. Knowledge about the qualification of equipment and instruments. Knowledge about regulatory guidelines and requirements. Knowledge about preparation and review of Development reports, validation reports and Dossier Location Hyderabad Apply to Job Send your resume to

Knowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolution apparatus for Tablets, Capsules, Oral Liquids and Oral Suspensions.USP Type-I, USP Type-II & USP Type-IV. Knowledge about the handling of analytical instruments like HPLC,GC, UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about the calibration of HPLC,GC,UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about regulatory guidelines and requirements. Knowledge about method transfer activities. Knowledge about the safety aspects. Knowledge about GLP and GMP. Knowledge about the qualification of equipment and instruments Location Hyderabad Apply to Job Send your resume to

Knowledge of about Preparation of Dossier. Sound knowledge of about semi regulated and regulated markets like USFDA , EU , MHRA , TGA , ANVISA , Canadian market. Knowledge of addressing regulatory deficiencies. Exposure to regulatory audits. Review of DMF. Knowledge of filling the products to semi regulated markets and regulated markets. Location Hyderabad Apply to Job Send your resume to