This document is a resume for Diana R. Riodeque, a 24-year old licensed Chemical Engineer with experience in research and development and quality control analysis. She received her Bachelor's degree in Chemical Engineering from Bicol University College of Engineering in 2014. Her work experience includes serving as an R&D Chemical Engineer at ARKRAY Industry, Inc. since 2016 where she develops clinical chemistry reagents and evaluates trial reagents, and working as a Quality Control Analyst at Sydenham Laboratories, Inc. from 2015 to 2016 where she performed analytical testing and maintained laboratory equipment. She is skilled in areas such as HPLC analysis, spectrophotometry, GLP, GMP, and preparing technical reports.

1. DIANA R. RIODEQUE
Chemical Engineer
Present Address:
Sto. Tomas, Batangas
Contact Number:
+639359545381
Skype:
facebook:diana.riodeque
Email Address:
diana.riodeque@yahoo.com
PERSONAL
INFORMATION
Date of Birth: May 8,1992
Place of Birth: Antipolo City
Age: 24
Sex: Female
SKILLS
AND QUALIFICATIONS
 Licensed Chemical
Engineer
 Knowledge in Microsoft
Office programs
 Knowledge in HPLC
analysis,
spectrophotometer and
other laboratory
equipment
 Knowledge in GLP,
GMP, HACCP and ISO
 Assay testing, titration,
preparation of reagents
and other laboratory
skills
 Preparation of technical
reports
A goal-oriented and dedicated chemical engineer with experience in
research and development and quality control analysis. Able to work
independently and with less supervision. Willing to work, be trained and
taught in any positions related to chemical engineering. Available for
relocation and shifting schedules if required.
WORK EXPERIENCE
R & D Chemical Engineer (Project-based)
ARKRAY Industry, Inc.
January 11, 2016-Present
 Development of clinical chemistry reagents
 Make experiment protocol
 Prepare materials including enzymes and/or coloring reagent for
trial production
 Prepare a sample (standard solution or serum/urine) to use for an
evaluation
 Check up prescription and production of trial reagents
 Measure and evaluate the trial reagents using clinical chemistry
instrument or spectrophotometer
 Data analysis and report using MS-Word or MS Excel
Quality Control Analyst
Sydenham Laboratories, Inc.
March 11,2015-January 8, 2016
 Strictly observe Good Laboratory Practices (GLP) and safety
standards in the performance of duty all times.
 Perform analysis on raw materials, in-process, bulk, intermediates
and semi-finished and finished product samples in accordance to
the test methodology and technical specifications.
 Operate HPLC, spectrophotometer machines and other laboratory
equipment, and maintain them in good conditions.
 Accomplish and submit the complete analytical report to the
supervisor.
 Check data conformances
 Prepare reagents required in the chemical testing and conduct
inventory of chemicals and consumablesreports to the supervisor if
inventory level of chemicals and consumables
 Participate in the validation and audit activities of the company
when required.
Reason for Leaving: Career Growth

2. EDUCATION
Bicol University College of Engineering
Legazpi City
2009 – 2014
Tabaco National High School
Panal, Tabaco City
2005 – 2009
Bantayan, Elementary School
Bantayan, Tabaco City
1999 – 2005
AWARDS AND HONORS RECEIVED
Chemical Engineering Licensure Examination Passer 2014
Career Service Professional Examination Passer 2013
Commission on Higher Education (CHED) Full Scholar 2009-2014
Class Valedictorian, Bantayan Elementary School 2005
SEMINARS ATTENDED
General Methods of Analysis
Sydenham Laboratories, Inc., Dasmarinas, Cavite
ISO, GMP, and HACCP Orientation
Sydenham Laboratories, Inc., Dasmarinas, Cavite
Good Laboratory Practices (GLP) and Laboratory Safety
Sydenham Laboratories, Inc., Dasmarinas, Cavite
2015
Seminar on Occupational Health and Safety Management
Occupational Safety and Health Center, Agham Road, Quezon City;
2012