Carlos A. Dávila Lorenzana
Estancias de Cerro Gordo, Plaza Mercedes 121
Vega Alta, Puerto Rico 00692
Seeking a position in the manufacturing environment.
Professional with initiative, adaptability, integrity, innovation, and teamwork oriented. Excellent interpersonal skills and good verbal and written communication skills both English and Spanish. Demonstrated technical knowledge in manufacturing and packaging activities. Computer literate with knowledge of Word, Excel, Project and statistical programs. Knowledge of manufacturing regulations ISO 9000, GMP, OSHA, ISO 1401, Six Sigma Champion Certificate, KRONOS and MP2. Strong costumer focus. Able to work under pressure, hand on working and handle multiple tasks.
2002 American University of Puerto Rico, Bayamon Campus
2006 Biotechnology Manufacturing Technology; Cell Culture and Fermentation.
Advance Professional Development Centre, Caguas PR.
1980 Digital Electronic Diploma, Miguel Such Vocational School, San Juan, PR
2009 –Actual – Manufacturing Supervisor , Temporary Contract –Biovail Laboratories, Carolina, PR. 787-***-****
In charge of Compounding, Beads, Granulating, Extruder, Weightlifting, Mixing, Oven areas, Encapsulation, Compressing, Coating, and Production lines Areas. Meet production requirements in accordance with production standards in full GMP compliance.
2003 – 2007 – Manufacturing Supervisor Compounding Area – Pfizer, Vega Baja Plant. 787-***-****
In charge of Compounding – Granulating area in the 3rd. shift, also coordinating manufacturing and quality activities in Weightlifting ( Pesaje), Mixing, Oven areas, Encapsulation, Compressing, Coating, and Production lines Areas, manufacturing Lipitor, Accupril, Neurontin, Lirica, Benadryl and others product over counter. Meet production requirements in accordance with production standards. Direct supervises of 20 operators, maintained in full GMP compliance through on the floor observation. Specific responsibilities include writing evaluating and approving reports, protocols and procedures. Investigation of quality deviation and manager performance indicator.
2002 – 2003- Manufacturing Supervisor, Clean Room and Packing.
Stryker Puerto Rico, Arroyo Plant. 939-***-****
In charge of Endoscopies Unit, Medical Devices. Lean Manufacturing Environment. Supervise 43 persons include operators, Materials handler, QC operator and packers. Responsible for productivity and quality line production in Clean Room and Packing, compliance all FDA regulations. Coordinate product shipping to Gamma and ETO. Trained and certificated of manufacturing associates in ISO 9000 and QSR Application.
1995 – 2002 Manufacturing Supervisor, Sub-Assembly, Production and Packing Areas. Cutler Hammer Eaton, Toa Baja, Plant .787-***-****
1980– 1995 Production Supervisor, QC Inspector Electronic, Technician. Intel de Puerto Rico Inc. Las Piedras Industrial Park, Las Piedras, P.R.
LICENSES & CERTIFICATE
-Right First Time method # 1- Pfizer
-Pharmaceutical Operations in Compounding – Granulating, Weightlifting, Mixing, Oven, Encapsulation, Compressing, Coating areas. - Pfizer
-Course on Solid dose Manufacturing Technology – Pfizer
-Introduction to Pharmaceutical Operations- Pfizer
-FDA Regulation – SPR
-Lean Manufacturing - SPR
-Six Sigma Certification - Eaton Quality Institute
-I S O 9000 & 14001 Regulation - Eaton
-G M P Regulation -Eaton
-OSHA Regulations- Eaton