Posted by on March 12, 19103 at 22:55:33:
ROXANNE L. MACUHA
Ph 3 Blk 3 Lot 10 Citihomes, Molino 4, Bacoor, Cavite 4102
Rm. 403 East Capitol Bldg. No. 7 East Capitol Drive, Bo. Kapitolyo, Pasig City 6103
Office - (02)6378975/73; (0916) 7323926; roxmacuha@yahoo.com
EMPLOYMENT HISTORY
Company Pharmacist
St. Carlos Pharma International, Inc.
Rm. 403 East Capitol Bldg. No. 7 East Capitol Drive, Bo. Kapitolyo, Pasig City
September 1998 – Present
Work Description:
1. Register all products (Drugs, Food Supplements) at the Bureau of Food and Drugs.
2. Monitors the validity of all Certificate of Product Registrations (CPRs) and Licenses to Operate (LTOs)
3. Handles all transactions with various government agencies that include Bureau of Food and Drugs, Department of Trade and Industry, and Dangerous Drugs Board
4. Coordinates with toll manufacturer on the products for research and development and manufacturing process
5. Handles importation of raw materials
6. Prepares documents, labels, and protocol for post-marketing surveillance of products for registration.
7. Manages procurement and purchase of raw materials, packaging materials, reference standards, and equipment from local and overseas sources
8. Research and provides information on drug products required for registration, manufacturing process and labeling purposes.
9. Manages controlled substances inventory and drug sample supplies.
BFAD Liaison Officer/Regulatory Affairs Officer
La Croesus Pharma, Inc.
Brgy. Sto. Tomas, Biņan, Laguna
June 1996 – August 1998
Work Description:
1. Register all products (Drugs, Food Supplements, Cosmetics, Veterinary Drugs, Household Hazardous Remedies) at the Bureau of Food and Drugs and Bureau of Animal Industry.
2. Monitors validity of all Certificate of Product Registrations (CPRs) and Licenses to Operate (LTO).
3. Handles all transactions with various government agencies that include the Bureau of Food and Drugs, Bureau of Animal Industry, Department of Trade and Industry, Department of Health and Dangerous Drugs Board.
4. Prepares all documents for product registration which involves: a) coordinating with the Quality Control Department on tests and procedures conducted on raw material, in process and finished goods, b) coordinating with the Research and Development Manager on new products for registration, products for development, and stability of all products, c) coordinating with the Quality Assurance Department and Technical Arts Department on labels and packaging materials.
5. Prepared and wrote Standard Operating Procedures on Drug Products which the laboratory uses up to now.
Company Pharmacist
Cresto Laboratories, Inc.
50-A E. Rodriguez Avenue, Quezon City
April 1995 – March 1996
Work Description:
1. Register all products at the Bureau of Food and Drugs.
2. Conducts raw material analysis, in-process and finished product analysis.
3. Maintains inventory and records of reference standard, products for stability, product profile and finished goods.
4. Supervises production of goods and ensures it is within schedule and production operations are running smoothly.
5. Inspects finished goods.
EDUCATIONAL BACKGROUND
Elementary
Barcenaga Central School 1979 – 1985
Barcenaga, Naujan Oriental Mindoro
High School
Holy Infant Academy 1985 – 1989
Calapan, Oriental Mindoro
College
University of the Philippines 1989 - 1995
Ermita, Manila, Philippines
B.S. Pharmacy
Graduate School
Jose Rizal University 1999 - 2001
80 Shaw Boulevard, Mandaluyong City
Master in Business Administration (18 units)
EXAMINATIONS TAKEN
Pharmacist Licensure Exam 89.13%
Civil Service Professional Exam 92.42%
National College Entrance Exam 98.00%
SPECIAL SKILLS
Computer literate (Corel Draw, MS Publisher, MS Word, MS Excel, MS Powerpoint, MS Paint), Internet
SEMINARS
1. Philamcare Basic HMO Training Program (August 2002)
2. Process Validation (March 2002)
3. Updates of the Dangerous Drugs Law (R.A. 6425, as amended) and its Implementing Board Regulations (August 30, 2000)
4. Process Validation, ISO 9000 and Plant Design (September 1999)
5. Information Technology in Pharmacy (July 1999)
6. Good Clinical Practice (March 1999)
7. Accreditation of Liaison Officers (October 1997)
8. GMP/Quality Management Systems/Validation and Computer Systems for Pharmaceutical Manufacture (June 1996)
9. Implementation of Admin. Order 56, Series 1989 Licensing of Drug Establishments/Outlets (June 1996)
PERSONAL DATA
Date of Birth : September 15, 1972
Place of Birth : Victoria, Oriental Mindoro
Height : 5'1
Weight : 100 lbs.
Civil Status : Single
Nationality : Filipino