M&A, restructuring and management in the chemical and pharmochemical areas.

Main responsibilities and achievements:Brazilian company, manufacturer of active pharmaceutical ingredients. Reporting to the Board composed of members-owners, 30 employees.Manager of all technical areas of the company, adjusting the industrial plant (Active Pharmaceutical Ingredients - API) for storage of raw material / intermediate / finished product, fresh and recovered solvents, production facilities for extraction and purification / clean area, quality control facilities and quality assurance, production and quality control equipment, utilities, storage and concentration of mother-liquors, production processes, personal and standard operating procedures for compliance with Good Manufacturing Practices.Setting priorities and goals for correction, maintenance and management status in accordance with Resolution RDC No. 249/05 of ANVISA, EMEA EU GMP Part II and USA FDA - ICH Q7.Great familiarity with national and international GMP inspections, and after appointment as Technical Director, I was responsible in the company for the conduct of work to comply with inspections MHRA / EDQM, USA-FDA and ANVISA. In addition to the audits for qualification of suppliers of large international companies such as Bausch & Lomb, Impax, Santen, etc.Successful performance to conduct and revert a suspension applied by the European governing body (EDQM / Romania Sanitary Surveillance Authority) providing the company's return to the European market in less than one year after taking over the mission.Obtaining various approvals and GMP certifications with the regulatory agencies and the Sanitary Surveillance: ANVISA, American (FDA / USA), European (EDQM & MHRA). In addition to the approvals and qualifications by major national and especially international clients.Acting as chemical responsible to CRQ IV region, responsible technician before municipal sanitary surveillance, CETESB and Fire Department for 18 years.

Main responsibilities and achievements:Manager of all productive sectors in the company.Experience of productive plant startup of active pharmaceutical ingredients from herbal source through solvent extraction, adapting the facilities, equipment, processes, personnel and procedures for compliance with Good Manufacturing Practices.Successful practice in standardization and adaptation of the production areas to meet the standards of the CRQ IV region, CETESB and Fire Department.Leader and facilitator of the productive areas in the company for suitability and compliance with Resolution RDC No. 249/05 of ANVISA, EU GMP Part II - EMEA and ICH Q7 - USA FDA.Representative of the production area before the national and international GMP audits and inspections.Practice and knowledge of storage and handling of flammable and corrosive gases and liquids.Conducting all work to meet the productive areas to inspections of USA-FDA and ANVISA. In addition to the audits for qualification of suppliers of large international companies such as Bausch & Lomb, Impax, Santen, Allergan, IVAX, etc.Successful management by the various approvals and GMP certification of production areas with the regulatory agencies and the Sanitary Surveillance such as the American (FDA / USA), European (Denmark). In addition to the approvals and qualifications by major national and especially international clients.Process improvements extraction and purification of an active pharmaceutical ingredient (API) plant source:• extraction process bottleneck solution (campaigns) solving the biggest problem of formation of emulsions, allowing the increase of subsequent steps and reduced downtime by 20%;• Solvent recovery, resulting in a 40-50% cost savings resulting from these inputs and ensuring the economic viability of the process;• Traceability and Bittern recovery of IFA salts purification process. Immediate increase of income of at least 30% with the reduction in production costs at the same rate.

Main responsibilities and achievements:Reporting to the Manager of the Electrochemical Department, 14 direct employees team. Sodium Chlorite production by electrolysis Supervision and byproducts.Coordination of the production area and the quality control in the Electrochemical Department, ensuring the smooth functioning of the process within the established quality parameters.Increased productivity and security due to adopted improvements and preventive maintenance.Performance in the release of the final product (Sodium Chlorite, Sodium Hypochlorite, Hydrogen, Caustic Soda, Sulfuric Acid, Brine, Chlorine, Hydrogen, etc.) and monitoring of intermediate products and raw materials (Sodium Chlorate, Hydrochloric Acid, Hydrogen Peroxide , Caustic Soda, Chlorine Dioxide, Sulfuric Acid, Brine, etc.).Release and maintenance of monitoring in confined spaces, at heights, hazardous chemicals pipes, reactors and tanks, pipes and equipment with flammable and explosive gases.10 % Reducing the number of accidents and the number of production stoppages due to good planning and supervision of preventive maintenance.

Reporting to the Head of Electrochemical Department, 14 employees staff. Assistance in Sodium chlorite production supervision (from electrolysis and redox reactions) and their by-products.The production area supervision and quality control of Sodium chlorite section.Increased productivity and security due to adopted improvements and preventive maintenance.Performance in the release of the final product (sodium chlorite, sodium hypochlorite, hydrogen) Caustic Soda, Sulfuric Acid, Brine, Chlorine, Hydrogen, etc.) and monitoring of intermediate products and raw materials (sodium chlorate, Hydrochloric Acid, Hydrogen Peroxide, Caustic Soda, Chlorine Dioxide, Sulfuric Acid, brine, etc.).

Reporting to the Head of Quality Control Central Laboratory.Knowledge and practice of sampling and analyzing raw materials and solvents in tank cars.Implementation of all the analyzes of industrial water used in the department of plant utilities and raw materials and end products of Electrochemical department.Preparation and factoring of analytics solutions provided to all productive sections with chemical laboratory at the plant.Calibration of volumetric glassware used in the Central Laboratory.Performing analysis of various products for use in R & D testing.