AURORITA BALLESTER PHAM
***** ***** ***, **** *** . Torrance, CA 90504 . 310-***-****
********.*********@*****.***
summary
A motivated, goal-oriented, hardworking individual. Extensive knowledge of
various laboratory functions, process, quality and safety requirements, and
general efficiency practices. Good communication and organization skills.
Demonstrates a basic knowledge of professional principles and skills.
Effectively uses fundamental concepts, practices, and procedures of
particular area of specialization.
work experience
University Park Healthcare Center
Los Angeles, CA Oct 2011 - present
Medical Records Department Head
. Maintains patient data when healthcare is provided.
. Ensures that information that the patient provides concerning their
demographic characteristics, history and extent of disease, diagnostic
procedures or treatment is accurate.
. Responsible for maintaining and securing all written and electronic
medical records that include the observations, medical or surgical
interventions and treatment outcomes, symptoms and medical history,
the results of examinations, reports of x-ray and laboratory tests,
diagnosis and treatment plans contained in the record is complete,
accurate and only available to authorized personnel within the
facility.
. Ensures that medical charts are completed and properly identified and
signed by responsible parties, nurses and physicians.
. Communicates with physicians and other healthcare professionals to
obtain additional information about patient.
. Collects data for medical research and for calculating facility
occupancy rates.
. Supervises, guides, motivates and evaluates personnel for the entire
department, which can include medical record technicians, medical
coding specialists, medical secretaries and file clerks all while
implementing department policies.
Dendreon
Seal Beach, CA Jun 2011 - Oct 2011
Quality Control Associate I
. Confirms the identity of sipuleucel-T and APC8015 by detecting the
presence of the PA2024 fusion protein and the identity of APC Placebo
product which does not contain PA2024 using a sandwich enzyme-linked
immunosorbent assay (ELISA).
. Determines the endotoxin levels in autologous cellular immunotherapy
products prior to release using the Kinetic-QCL kinetic-chromogenic
assay by measuring the chromophore released from a suitable
chromogenic peptide by the reaction of endotoxins with the LAL reagent
from the onset time needed to reach a pre-determined absorbance of the
reaction mixture.
. Prepares, stains, observes and qualifies a Gram stain slide which is
used as a safety test for the rapid determination of the presence of
microbial contamination to classify bacteria on the basis of their
Gram stain reactions and cellular morphology.
. Determines the complete blood count for active immunotherapy samples
using an automated Beckman / Coulter AcT 5 Diff Cap Pierce Hematology
Analyzer.
. Determines viability of active immunotherapy samples using the Trypan
Blue Exclusion Method that live cells possess intact cell membranes
that excludes certain dyes, such as Trypan Blue, whereas dead cells do
not. A viable cell will have clear cytoplasm whereas a non-viable
cell will have blue cytoplasm.
. Performs Quality Control inspection of the leukapheresis collection
units for use in manufacturing of active immunotherapy products.
. Operates and performs routine and preventative maintenance of Becton
Dickinson FACSCalibur flow cytometers and Beckman Coulter FC500
Cytometry System.
. Operates and performs routine and preventative maintenance of the
Coulter AcT 5 Diff Cap Pierce Hematology Analyzer.
. Operates and performs maintenance of the Bio-Tek Absorbance Microplate
Reader, Model ELx808 used in the Quality Control laboratory.
. Operates, maintains and cleans upright and inverted compound light
microscopes used in the Quality Control laboratory for the
visualization and analysis of cells, microorganisms and other
microstructures, utilizing both brightfield and phase-contrast
microscopy.
. Complies with Standard Operating Procedures, Test Methods, Good
Manufacturing Practices and Good Documentation Practices.
Siemens Healthcare Diagnostics
(Formerly Diagnostic Products Corporation)
Los Angeles, CA Mar 2005 - Jun 2011
Biochemist I
. Operates the Immulite Immunoassay System 1, Immulite Immunoassay
System 1000, Immulite Immunoassay System 2000 and Immulite Immunoassay
System 2500 for testing products in the Allergy Department.
. Provides assistance in research, analysis, and experimentation for
product and process development of immunoassays.
. Performs routine tests following written protocols and SOPs related to
the research and development of new Allergens.
. Performs basic dilutions and calculation for Multi-Serum Evaluation
and Titering of allergens.
. Performs Method Comparison, Inhibition, Linearity and Stability on
Analyte Specific Reagents.
. Work closely with scientist to determine future assignments.
. Review, analyze and summarize data for Multi-Serum Evaluation and
Titering of allergens.
. Monitors and evaluates Immulite Immunoassay System performance.
. Manages troubleshooting and performs preventative maintenance of
laboratory equipment and proper documentation.
. Submits Immulite Immunoassay System monthly reports to the manager.
. Manages inventory of Immulite Immunoassay System supplies and
laboratory supplies.
. Performs calibrations on laboratory equipments.
. Maintains documentation on maintenance of Immulite Immunoassay System
and on calibrated equipments.
. Responsible for training new employees.
Laboratory Corporation of America
(Formerly Genzyme Genetics)
Los Angeles, CA Jul 2008 - Jun 2011
Accessioner II (Part-time)
. Prepares laboratory specimens for designated departments prior to
laboratory analysis and testing.
. Unpacks specimens from branches or ports and routes specimens by type
to various staging areas.
. Resolves and documents problem specimens.
Specialty Laboratories
Valencia, CA Apr 2001 - Mar 2005
Clinical Laboratory Associate
. Assists Clinical Laboratory Scientist in the Automated Chemistry
department by operating the Advia Centaur Immunoassay System for
testing.
. Performs consistently a high volume of clinical tests.
. Responsible for pulling specimens from storage.
. Prepares and tests controls and evaluates their usefulness based on
standard criteria.
. Performs test calibrations and runs Quality Control material at
appropriate intervals.
. Checks the computer review reports to monitor accurate reporting of
laboratory results.
. Responsible for performing preventative maintenance of laboratory
equipment and proper documentation.
. Monitors and maintains a consistent supply of reagents and
consumables.
Senior Specimen Processing Coordinator
. Receives incoming specimens and ensures specimen's integrity by
verifying identification and verifying the appropriate samples were
submitted given the requested tests.
. Processes large volumes of incoming specimens within time limits.
. Responsible for training new employees.
SunBridge Care and Rehabilitation
Playa del Rey, CA Jun 1999 - Apr
2001
Medical Records Assistant
. Assists Medical Records Director by doing audits and other tasks
assigned by MRD.
. Responsible for maintaining health information and / or medical
records.
. Understands and monitors applicable regulations, policies and
procedures.
Central Supply Manager
. Responsible for ordering, inventory, distribution of central and
medical supplies and for management of medical equipment while staying
with budget guidelines.
Data Entry Clerk
. Assists Case manager / MDS Coordinator in data entry of resident's
Minimum Data Sheet.
eDUCATION
Bachelor of Science, Medical Technology
Angeles University Foundation
Angeles City, Philippines
June 1994 - September 1998
Clinical Internship Program
James L. Gordon Memorial Hospital
Olongopo City, Philippines
October 1997 - March 1998
Angeles University Foundation Medical Center
Angeles City, Philippines
April 1998 - September 1998