KRISSIA CAMILLE RODRIGUEZ
BACHELOR OF SCIENCE IN PHARMACY
Bocaue
Summary
Detail-oriented Pharmaceutical Quality Control Analyst with over 5 years of experience in GMP-regulated environments, specializing in HPLC/UPLC, GC, UV-Vis, and dissolution testing. Proven ability to perform accurate analysis, interpret complex data, and maintain high standards of documentation and compliance. Experienced in OOS investigation, method validation, and stability studies. Committed to ensuring product quality, safety, and regulatory compliance.
Overview
5
5
years of professional experience
Work History
Quality Control Analyst
New Myrex Laboratories Inc.,
11.2023 - 04.2026
- Performed routine and non-routine analysis of raw materials, in-process samples, and finished products
- Prepared and reviewed Certificates of Analysis (COA) and laboratory reports
- Contributed to method validation and stability studies
- Developed and implemented procedures to meet product quality standards.
- Performed routine maintenance and calibration on testing equipment.
- Recorded and organized test data for report generation and analysis.
- Conducted data review and followed standard practices to find solutions.
- Provided training to new hires on quality control procedures, fostering a culture of excellence within the team.
- Maintained a safe working environment, adhering to safety regulations and proper handling of hazardous materials.
- Conducts laboratory test based on official or adopted methods of analysis using HPLC / UPLC instruments and generates analytical reports.
- Performs HPLC / UPLC analysis of products according to schedule.
- Performs mathematical calculations based on raw laboratory data.
- Reviews HPLC / UPLC chromatograms and reports to immediate Supervisor any deviation noted.
- Maintains records of QC test results and logs data in the monitoring log sheet.
- Maintains fresh stock of reagents, test solutions and mobile phase solutions for analysis as well as records of preparation and follows guidelines set for its proper storage disposal.
- Calibrates, cleans and maintains equipment and instrument.
- Maintains updated records of instruments calibration.
- Assures substances tested are disposed of properly and safety.
- Assists in chemical waste disposal.
- Calibrates In – House Standard vs USP Standard / EP Standard.
- Performs responsible in accomplishing testing reports and/or Certificate of Analysis every after analysis.
- Effectively performs assay, organic impurities, dissolution, product testing and analysis of Raw Materials, Process Validation, In – Process, Finished Products and Stability using various instruments.
- Maintains high quality laboratory documentation in accordance with SOP’s and GDP guidelines.
- Adheres to Departmental Standard Operating Procedures and Work Instructions based on cGMp, cGPL, ISO guidelines and complies with proper safety regulations.
Jr. Quality Control Analyst
Lloyd Laboratories Inc.,
06.2016 - 06.2019
- Performed routine and non-routine analysis of raw materials, in-process samples, and finished products
- Prepared and reviewed Certificates of Analysis (COA) and laboratory reports
- Contributed to stability studies
- Developed and implemented procedures to meet product quality standards.
- Performed routine maintenance and calibration on testing equipment.
- Recorded and organized test data for report generation and analysis.
- Conducted data review and followed standard practices to find solutions.
- Provided training to new hires on quality control procedures, fostering a culture of excellence within the team.
- Maintained a safe working environment, adhering to safety regulations and proper handling of hazardous materials.
- Conducts laboratory test based on official or adopted methods of analysis using HPLC / UPLC instruments and generates analytical reports.
- Performs HPLC / UPLC analysis of products according to schedule.
- Performs mathematical calculations based on raw laboratory data.
- Reviews HPLC / UPLC chromatograms and reports to immediate Supervisor any deviation noted.
- Maintains records of QC test results and logs data in the monitoring log sheet.
- Maintains fresh stock of reagents, test solutions and mobile phase solutions for analysis as well as records of preparation and follows guidelines set for its proper storage disposal.
- Calibrates, cleans and maintains equipment and instrument.
- Maintains updated records of instruments calibration.
- Assures substances tested are disposed of properly and safety.
- Calibrates In – House Standard vs USP Standard / EP Standard.
- Performs responsible in accomplishing testing reports and/or Certificate of Analysis every after analysis.
- Effectively performs assay, organic impurities, dissolution, product testing and analysis of Raw Materials, Process Validation, In – Process, Finished Products and Stability using various instruments.
- Maintains high quality laboratory documentation in accordance with SOP’s and GDP guidelines.
- Adheres to Departmental Standard Operating Procedures and Work Instructions based on cGMp, cGPL, ISO guidelines and complies with proper safety regulations.
Education
Bachelor's Degree - Pharmacy
Our Lady of Fatima University
Marulas, Valenzuela City10-2015
Secondary - undefined
Colegio de Santa Maria
Bagbaguin Sta. Maria Bulacan01-2010
Primary - undefined
Colegio de Santa Maria
Bagbaguin Sta. Maria Bulacan01-2006
Skills
ATR-FTIR Analytical Skills Atomic Absorption Spectrophotometry Autotitrator Calibration Chemical Testing Chemistry Communication Computer Literacy Creative Problem Solving Data Analysis Disintegration Dissolution Testing FTIR Finished Product Finished Product Analysis Friability testing Good Laboratory Practice (GLP) High-Performance Liquid Chromatography (HPLC) In - process Analysis In - process Testing Karl Fischer Titration Laboratory Equipment Laboratory Safety Laboratory Technicians Manual Titration Medication Dispensing Method Development Micropipette Moisture Analysis Muffle Furnace New Product and Method Development Patient Counseling Physical Testing Quality Control Raw Materials Raw Materials Analysis Reagents Self Learning Skilled Multi-tasker Spectroscopy Stability Analysis Stability Testing Standard Operating Procedure (SOP) US Pharmacopeia (USP) UPLC UV/Vis Spectroscopy pH meter
Work Availability
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Timeline
Quality Control Analyst
New Myrex Laboratories Inc.,
11.2023 - 04.2026
Jr. Quality Control Analyst
Lloyd Laboratories Inc.,
06.2016 - 06.2019
Secondary - undefined
Colegio de Santa Maria
Primary - undefined
Colegio de Santa Maria
Bachelor's Degree - Pharmacy
Our Lady of Fatima University
PERSONAL PROFILE
- Age: 31
- Gender: Female
- Birthday: June 06, 1994
- Nationality: Filipino
- Religion: Roman Catholic
- Civil Status: Married
- Height: 5'2
- Weight: 134 lbs
PERSONAL PROFILE
- Age: 31
- Gender: Female
- Birthday: June 06, 1994
- Nationality: Filipino
- Religion: Roman Catholic
- Civil Status: Married
- Height: 5'2
- Weight: 140 lbs