Experience in development and validation of analytical methods for raw materials and finished products, applied to the development of new products and industrial support, aligned with RDC 166/2017 and RDC 53/2015 and using the analytical techniques HPLC, CG spectrophotometry UV / VIS, dissolution, and potentiometric titration.Experience in developing analytical methods indicative of stability applying AQbD (Analytical Quality by Design). Forced degradation profile studies aligned with RDC53/2015 and elaboration of the degradation profile report encompassing bibliographic review, predictive analysis and discussion of results. Elaboration of protocols and reports of analytical validation acting directly with elaboration and revision of specifications and analytical methods. Validation and development of analytical methods for cleaning validationKnowledge of GLP, GMP, Legislation and Pharmacopoeias.

Experience in analytical validation and analytical transfer of raw materials, finished products methods, by HPLC (Shimadzu / Waters), UV / VIS and IR spectrophotometer, TLC and dissolution. Forced degradation studies of drugs to adapt analytical methods to RDC 899/2003, RDC 58/2013 and CP 68/2014 for the registration of new drugs and renewal of portfolio registration. Verification and updating of analytical methodology according to official compendia and analytical data from validation of analytical methodology. Validation and development of analytical methods for cleaning validation. Analysis for process validation. Conference of documentation and analytical data, as well as protocols and reports of validation of analytical methodology. Responsible for the purchase and inventory control of standards and reagents.Knowledge of GLP, GMP, Legislation and Pharmacopoeias.

Experience in analytical validation analytical transfer of raw materials and finished products methods by HPLC (Agilent HP) and spectrophotometer (UV / VIS). Improvement of analytical methods applying dissolution profile and HPLC analysis. Study of API degradation and stability studies for processes of registration of new drugs and renewal of portfolio registration. Verification and updating of analytical methodology according to official compendia and analytical data from validation of analytical methodology. Conference of documentation and analytical data, as well as protocols and reports of validation of analytical methodology

Experience in analysis of finished drugs, stability study analysis, physico-chemical tests, analyses with the dissolutors Erweka and Pharma Alliance, analyses performed by UV spectrophotometers, atomic absorption by Spectr AA Varian and infra-red, analyzes performed by HPLC (High-performance liquid chromatography) belonging to the brands LaChrom, LaChrom Elite, Agillent, Waters Millenium (Empower Software), Waters (Software Empower 2) and analyses performed by CG Agillent.

Raw material analyses, drug stability analyses, analyzes carried out by titration, UV spectrophotometers, atomic and infrared absorption, physical-chemical tests in general, such as density, pH reading, humidity, average weight, viscosity.