Quality Assurance Technician

LOURDES ARRIOLA

*** ******* **** ***. *

Phone: 201-***-****

Eatontown, NJ 07724 Email:

************@*****.***

POSITION APPLIED FOR: Analytical Chemist - Method Development/Validation

Objective : To obtain a position that will utilize my

pharmaceutical laboratory skills and experience

Education : Centro Escolar University - Bachelor of Science in

Pharmacy - Manila, Philippines

: Philippine Women's University -Masteral units in Clinical

Pharmacy - Manila, Philippines

SKILLS

. Extensive experience in analytical instrumentation such as HPLC, FTIR,

UV-Visible Spectropho-

tometer, Dissolution Apparatus (Apparatus 1, 2, &3), Disintegration

Tester, AAS, KF, Oven, scales and balances, pH meter, Tablet Testing

Machine, Viscometer, Friability Tester, GC

. Good understanding of GLP, Regulatory Compliance, cGMP and Good

documentation

. Good knowledge in physical and chemical testing of drug substance and

drug products

Certification : Certified Pharmacy Technician (National)

License : New Jersey License Pharmacy Technician

Job Experience:

July 2008 -to- November 16, 2012 : Westward Pharmaceuticals - QC

Chemist

. Performs stability tests and chemical/physical analyses of both

In-process and finished products. I have thorough knowledge of

USP (United States Pharmacopoeia), NF (National Formulary) and BP

(British Pharmacopoeia). To perform the projects assigned to me,

I use different laboratory instrumentation (HPLC, UV, GC, IR, KF,

etc.) and wet chemistry techniques

. Participates in an Out-Of-Specification and Analytical Deviation

laboratory investigation

. Compiles data for documentation of testing and preparation

reports

. Works in both GLP and GMP environment and ensure regulatory

compliance

. Interface with Operation, R&D, and Quality Assurance

May 2007 -to- July 2008 : Westward Pharmaceuticals - QA Production

Inspector

. Performs quality inspection of incoming finished products by

performing required visual

and functional tests

. Identifies problems and issues regarding quality of products and

makes recommendations

. Performs batch record review, random sampling and in-process

testing, final AQL visual inspection of finished bulk products

. Verifies line clearance for dispensing, manufacturing and

packaging activities

review pharmacy stage BMR

. Verifies the cleanliness of the rooms and equipments

. Checks Material Data Sheets of every product prior to

manufacturing

. Verifies manufacturing activities and reviews of manufacturing

BMR at granulation,

Compression and coating encapsulation end stage

. Blend sampling using Sampling Thief

. Collects stability sample

. Reviews and releases the batch for packaging/finishing

. Affixes/Removes QA disposition labels on the drug/product

containers

. Checks bulk RMs at Pharmacy Dept. based on FMOM

. Check operators for proper uniform

Abbott Laboratories, Philippines - Sr. Chemical and Microbiological

Analyst

. Performs chemical/physical analyses of in-process and finished

products

. Performs stability tests to determine efficacy and shelf life of

finished products

. Updates QA records such as assay reports, standard control and

testing procedures and product specifications

Draws sample materials on received RMs based on standard

sampling procedures

. Performs identification and chemical tests based on standard

test procedure

Contact this candidate