Describe casi toda mi hoja de vida, tanto las experiencia academicas cientificas y experiencias profesionales tanto en Peru, Espana y USA.

1. P a g e | 1. LUIS ENRIQUE MEDINA MEDINA / 3311 Mission Street, San Francisco, CA 94110 / Ph: 4158947863
PhD. LUIS ENRIQUE MEDINA MEDINA
luiggim65@hotmail.com/luiggim65@usal.es
I.-Highly Qualified Pharmaceutical Chemist Specialized in Pharmacy
I have more than 10 years of experience working first as Technical Director and Management of Pharmaceutical
Offices, Pharmacies, Drugstores, Distributors, employing for it the requirements of law of the Ministry of Health of
the General Direction of Medicines Food and Drugs. Second, I have more than 10 years of having worked in as
Chemist Pharmaceutical Analyst and Chemical Expert of Raw Material of the national center of quality control of
the National Health Institute, Peru. Performing and applying various Analytical Techniques for Analysis such as:
Gravimetric Techniques, Spectrophotometric (UV/IR/FMT/Atomic Absorption), Chromatographic
(HPLC/DAD/CCF/CG/CA), Colorimetric, for which he applied in the tests of Identification, characterization, content
and dissolution of active ingredient of pharmaceutical products. Applying the analytical methods of the official
works such as: USP, BP, FM and Technical of own laboratories. As a chemical expert and with 5 years’ experience in
the identification of narcotics such as: cocaine, heroin, and marijuana we work on the basis of the official USP work
requested by the Ministry of the Interior. I have also developed numerous researches works with experience in the
monitoring of clinical trials and Drug Dissolution Profiles of brand versus generic drug and also referred to the
Integrated Quality System, Analytical methods, publication in Journals and Journals on Immunocytochemical at the
brain tissue and neuronal techniques.
II.-Professional Strengths
Bilingual Spanish, English/ High Academic Training. English language level 4 and ESL 184 College of San
Francisco, CA, USA. / Bs Pharm, Master D, PhD Pharmacy.
Knowledge and experience of working with Official
Quality Standards
In Pharmaceutical Industry, and Labs Quality C. ISO 17025.
ISO 9001, ISO 14001, ISO 18001 and OHSA/TQM.
Management of Software in the Pharmacy Office. Farmaplus, Farmanager, Bots Plus web 2.0 and Nixfarma
and MS Office.
Proven Analytical Capability / Clinical Trials Monitor. INS from Peru, certification and quality Assurance.
Chemical Expert of the Ministry of Health
Management and Advisor of Enterprises as Technical
Director.
Pharmaceutical Offices, Apothecaries and Drugstores,
Distributors and Laboratories.
Knowledge of Analytical Techniques of
Pharmaceuticals for Drugs, Medications, Raw material
and Foods /Quality control.
Knowledge of USP methods USP/BP/NF/TLC/HPLC/DAD
Spectrophotometer UV/VIS/IR/Fluorometry.
Research Experience in Peru and Spain Publications of
work scientists and Websites Slides.
Journal of Chemical Neuroanatomy
Folia Histoquemica et Cryobiological
III.-Professional Experience Lima, Peru and Spain
3.1.-Experience’s Work in Pharmaceutical Offices, Apothecaries and Drugstores, Distributors and Laboratories.
Of April, 1995 to 2000 - Experience in Peru
Companies Title Position
• Apothecary "Clarita Regent and technical adviser"

2. P a g e | 2. LUIS ENRIQUE MEDINA MEDINA / 3311 Mission Street, San Francisco, CA 94110 / Ph: 4158947863
• Apothecary "Balani" Advisor technical and vocational
• Peruvian Institute of security-in-charge of the pharmacy service.
Social IPSS and pharmacological Committee - Regent of Service Pharmacy
• Apothecary "Delia" Regent and Technical Adviser
• Pharmacy San Luis Regent and Technical Advisor.
Functions and procedures
➢ Control and supervise the sale of products.
➢ Verify and control that the dispensing of prescriptions is carried out in accordance with what is
established in Chapter IV of the regulations.
➢ Acquire, guard and control the sale of drugs for medical use subject to control.
➢ Provide and control that the dispatch of medicines, when their sale is carried out in a fractional manner,
complies with the provisions of these Regulations.
➢ Prepare and / or supervise the preparation of magisterial and official formulas, in accordance with the
provisions of Article 34 of these Regulations.
➢ Oversee that the storage system for pharmaceutical and related products ensures their conservation,
stability and quality and, in the case of controlled products, their safety.
➢ Intervene in the selection of the inputs used in the preparation of magisterial and official formulas.
➢ Train, train and permanently supervise the assistant and auxiliary person in the correct performance of
the storage and dispensing functions.
➢ Verify that contaminated, adulterated, falsified, altered or expired products are withdrawn from sale and,
when appropriate.
➢ Maintain the prescription, drug control and occurrence book updated; k) Report any adverse drug
reactions known to it, in accordance with the provisions of Articles 136 and 139 of the Regulation for
Health Registration, Control and Surveillance of Pharmaceutical Products and Products.
➢ Prepare and present the balances referred to in the Regulation of Narcotic Drugs, Psychotropics and other
Substances subject to Sanitary Control. Visibly carry, while developing your work, a credential with your
name, profession, registration number and position.
3.2.- Experience’s Work in Pharmaceutical Offices, Apothecaries and Drugstores, Distributors and Laboratories.
Of November, 2009 to 2016 - Experience in Spain
A.-Pharmacy "HERMINIA Mª JESÚS MARTÍNEZ" – ASTURIAS, Spain 2006
o Position: Pharmaceutical Assistant-Program of handling FARMA II MIL
o Time August 2006 - November 2006
o Management of the Pharmaceutical Management Information Programs: Nixfarma, Farma 2000.

3. P a g e | 3. LUIS ENRIQUE MEDINA MEDINA / 3311 Mission Street, San Francisco, CA 94110 / Ph: 4158947863
• Function: Pharmaceutical care of green and red prescriptions, active and retired.
• Warehouse management and orders and receipt of orders Distributors and Cooperatives. Guidance and
dispensing of recipes. Management of controlled medications.
B.-Pharmacy: MAGDALENA SANZ MILLÁN- San Adrian Navarra, Spain, 2007
o Job title: Substitute pharmacist from September 5 to September 30, 2007
o Pharmaceutical care of green and red prescriptions, active and retired.
o Warehouse management and orders and receipt of orders Distributors and Cooperatives. Guidance and
dispensing of recipes. Management of controlled medications.
o Management of the Pharmaceutical Management Information Programs Nixfarma, Farma, 2000
C.-Pharmacy: Eulogio Pardo Garde, Mendavia Navarra, Spain
o Position: Substitute Pharmaceutical Position in Operation, from July 1, 2017 to October 15, 2017.
o Function: Dispensation, description of paper and electronic recipes, management of stocks, management of
stocks, management of warehouse of hygienic products and toilet, counter service, health counselor in said
locality.
o Farmanager electronic prescription management and order management, stock review, Dispensation. Handling
and Nixfarma Pharmaceutical Management and electronic prescription. Management of Farmanager computer
programs.
D.-Professional Practices by agreement of the Master Degree of the University of Seville and the Farmaceutico
Fernandez y Canivell, S.A. laboratory (Malaga), Spain 160 hours from Monday to Friday. year of May 2016.
E.-Company: Devogest Levante, S.L. Murcia, Spain June, 2009 to 2014
Director Technical Pharmacist in integrated systems from November 2009 until November 2011, integrated
management of quality: ISO 9001, ISO 14001.
Functions:
• Management of expired drug files in all its Pharmaceutical forms.
• Reading of albaran by each supplier at the province of Murcia.
• Management of medical waste in all its Pharmaceutical forms.
• Collection, evaluation and final report of your technical file.
• Coordination with suppliers for waste management services for each type of medicine.
• Management of computer software and hardware packages for the classification of drugs and suppliers.
• Management of Standard Operating Procedures of Work.
• Management of the Integrated Quality System.
• Participation in Internal and External Quality Audits in compliance with ISO 9001, ISO 14001, ISO 18001.
F.-Drugstore: Devogest Levante, SL. Director Technical Pharmacist, March to May 2012. Position: Tecnical Advisor
of Drugstore

4. P a g e | 4. LUIS ENRIQUE MEDINA MEDINA / 3311 Mission Street, San Francisco, CA 94110 / Ph: 4158947863
Function:
• Provide the distributor with equipment equipped with personal, material and Technical means to
guarantee the correct conservation and distribution of the medicines.
• Guarantee the general or particular conditions for the preservation of medicines and especially the
maintenance of the cold chain throughout the distribution network through standardized procedures.
• Maintain a minimum stock of medicines that guarantee adequate continuity of supply. • Ensure delivery
times, minimum frequency of deliveries, permanent technical-Pharmaceutical advice and means of
support for pharmacy offices and services.
• Processing and Management of Standard Operating Procedures Affair for the Management of
Distribution, Dispensing of Medications, Distribution of Operational Área, Storage Área according to BPA
Techniques, BPD.
3.3.-Expert Chemist of the National Center of quality Control of the National Institute of health of the Ministry of
health of Peru.
Functions and procedures
• Develop the laboratory samples necessary for the analysis and Prepare test solutions for reference and
use.
• Record of essential data acquired during the process and report the information to the personnel
involved.
• Submit request for replacement supplies if necessary and maintain and manage a clean and orderly work
environment.
• Develop and install LC, HPCL, Gas Chromatography columns and Chromatographic column washing.
• Validation of Analytical Methods: HPLC, Volumetric, Stoichiometric, Spectrophotometric.
• Prepare for routine repairs and change laboratory instruments as needed for maintenance.
• Prepare standard and sample solutions as required by test methods.
• Perform physical-chemical analysis (i.e. pH, water content, loss on drying, melting point, density / specific
gravity, friability, tablet hardness, dimensions, disintegration, uniformity of dosage units and particulate
matter in the injections).
• Maintain proper documentation as required by laboratory SOPs.
• Comply with good cleaning and safety and hygiene practices.
• Assist in the optimization of analytical methods to quantify pharmaceutical products.
• Evaluation of information to determine compliance with standards: use relevant information and
individual judgment to determine whether events or processes comply with laws, regulations or
standards.
• Participation in external quality control programs (EQCP) developed by the WHO and USP.
• Participate and write the multiple Operating procedures analytical work in laboratories under his charge.