Ronald Pérez Medina
Phone: 787-***-****
***********@*****.***
OBJECTIVE
To work in your Company as a Licensed Chemist or related areas in which my experience and education can be applied and where professional growth will be encouraged in order to take part on corporate future plans.
WORK EXPERIENCE
Nov 2007 – Jan 2010
APP Pharmaceuticals Barceloneta, PR 00617
Laboratory Supervisor (Raw Materials)
Supervise analysts carrying out testing related to Raw Materials and Packaging Components and assure the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality products. Perform laboratory investigations when questionable analytical results have been generated. Review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications. Conduct personnel hiring, training and performance reviews.
May 2007 – Oct 2007
Wyeth Pharmaceutical Guayama, PR 00785
Laboratory Supervisor (Raw Materials)
Supervise analysts carrying out testing related to Raw Materials and assure the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality products. Perform laboratory investigations when questionable analytical results have been generated. Review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications. Conduct personnel hiring, training and performance reviews.
May 2005 – Feb 2007
Bristol-Myers Squibb Manatí, PR 00674
Laboratory Supervisor (Raw Materials)
Supervise analysts carrying out testing related to Raw Materials and assure the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality products. Perform laboratory investigations when questionable analytical results have been generated. Review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications. Conduct personnel hiring, training and performance reviews.
Dec 2002 – May 2005 Ortho Pharmaceutical (J&J) Manatí, PR 00674
Laboratory Supervisor (Raw Materials, Solids and Semi-Solids)
Supervise analysts carrying out testing related to Raw Materials, Solids and Semi-Solids products and assure the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality products. Perform laboratory investigations when questionable analytical results have been generated. Review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications. Conduct personnel hiring, training and performance reviews.
Jul 2002 – Dec 2002
Schering-Plough Manatí, PR 00674
Senior Analyst (Back-Up Supervisor)
Help supervisor with the testing scheduling, perform laboratory investigations when questionable analytical results have been generated and review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications.
Nov 1997 – Jul 2002
Warner-Lambert/Pfizer Vega Baja, PR 00694
Analyst
Perform chemical test such as assay, content uniformity and dissolution test to oral finished and stability products by using HPLC (Waters, Alliance, HP1100, HP1090, HP1050, Shimatsu), GC-FID (HP6890), pH Meter’s, UV-VIS, FTIR, Karl Fisher and Dissolution techniques. Perform product transfer and method validation activities. Perform data verification and testing schedules.
Oct 1995 – Oct 1997
Abbott Diagnostics Inc. Barceloneta, PR 00617
Solution Preparation Technician
Perform the manufacture of solutions (Bulks) under aseptic conditions that were filled in vials kits that are used in the clinical laboratories.
CAPABILITIES
• Good in “wet chemistry”, solution preparation and in instrumental methods of analysis.
• Knowledge on the use of AAS, HPLC’s (Waters, HP1100, HP1090, HP1050, Alliance and other’s), GC-FID (HP6890), pH Meter’s, UV-VIS, FTIR, KF and Balances.
• Perform chemical test such as assay, content uniformity and dissolution test to oral finished and stability products (solid dosage form).
• Knowledge on the calibration of all type of Balances, Dissolution Bath’s and UV/VIS.
• Qualification (IQ, OQ, PQ, LOD, LOQ and Linearity’s) and Preventive Maintenance of HPLC.
• Strongly knowledge on HPLC troubleshooting.
• Knowledge of GMP’s, GLP’s, SOP’s, MSDS’s, USP, EP, etc.
• Writing and/or review of SOP’s.
• Knowledge on the use of computer programs like Windows, Words, Excel, Power Point, Track Wise, SAP among others.
• Strong knowledge on programs for chromatographic data acquisition like Peak Pro, Chem. Station, Millennium (Empower) and ATLAS.
• Review and/or approve chemical and physical testing of materials and products in accordance with all applicable compendia and specifications.
• Conduct personnel hiring, training and performance reviews.
• Supervise analysts carrying out testing related to Raw Materials, Packaging Components, Solids and Semi-Solids finished products and assure the compliance to all quality control policies, procedures and systems to ensure the timely release of high quality products.
• Perform laboratory investigations when questionable analytical results have been generated.
• Fully bilingual (English or Spanish).
EDUCATION
Aug 1989 – Jun 1997
Universidad de Puerto Rico – Río Piedras, PR
BS in Chemistry
PROFESSIONAL MEMBERSHIP
• Active member of Colegio de Químicos de Puerto Rico.
• Chemist License Number 4371 from State Department, Puerto Rico Commonwealth Government.
REFERENCE
Available upon request.