DAYA RABADIYA
Brantford
Summary
Driven QC Chemist with a robust history in pharmaceutical quality control, notably at all my previous workplaces. Expert in HPLC, GC, and compliance with FDA and Health Canada guidelines. Demonstrates a keen ability to enhance team success and lab efficiency through meticulous analysis and procedural improvements. Excelled in handling complex analytical tasks and instrumental maintenance, showcasing strong analytical acumen and collaborative skills.
Overview
13
13
years of professional experience
Work History
QC, ANALYST 2
Germiphene Corporation
01.2023 - Current
- Analysis of Raw material, Finished product and Stability samples with report work
- Instrument used- HPLC (Empower2, Empower3)
- Gas Chromatography, Auto Titrator, Ph meter, IR
- UV Specrtrophotometer, Viscometer,Floride taster
- Wrote and revised standard quality control operated procedures
- Reviewed tested data in all relatable logbooks, reports and instruments.
QUALITY CONTROL CHEMIST
Bora Pharmaceutical
07.2022 - 01.2023
- Performed testing and quality control using approved laboratory procedures and instrumentation
- Deep knowledge of LIMS
- Physical test of liquid product like foreign particle matter, particle size, ph and weight of content
- Assay, RS, Dissolution, Content Uniformity of finished product and stability samples analysis on HPLC
- Maintained analytical instrumentation and laboratory equipment to maximize availability and functionality
- UV, IR, HPLC Agilent ,Empower 3, Chemstation software.GC (Perkin Elmer Clarus 580 Headspace Turbomatrix 40) , stability chambers, Dissolution Tester, Viscometer, homogenizer, specific gravity and wet chemistry techniques as per SOP
- Performed raw material analysis, cleaning Validation, analytical method validation
- Review of ROA and verification of logbooks
- Handling of Lab event, Deviation, Change Control, OOS, OOT and close it and Inform QC Head in case of any Deviation and Out of Specification observed.
QUALITY CONTROL ANALYST
Genvion Corporation
06.2021 - 06.2022
- Calibrate, maintain and troubleshoot lab equipment instruments to keep equipment fully operational
- Performed testing and quality control using approved laboratory procedures and instrumentation
- Assay, RS, Dissolution, Content Uniformity of finished product and stability samples analysis on HPLC
- UV, IR, HPLC Agilent ,Empower-2&3, Chemstation software.GC (Perkin Elmer Clarus 580 Headspace Turbomatrix 40), stability chambers, Dissolution Tester, Viscometer, homogenizer, specific gravity and wet chemistry techniques as per SOP
- Performed raw material analysis, cleaning Validation, analytical method validation
- Review of ROA and verification of logbooks
- Handling of Lab event, Deviation, Change Control, OOS, OOT and close it and Inform QC Head in case of any Deviation and Out of Specification observed
- Calibration activities of various instrument HPLC,UPLC, UV Spectrophotometer, KF and IR
- Sampling and analysis of in-process, and finished products, Stability Study & investigational samples
- Assay, Impurities, Content Uniformity, Loading, Release, IR,Retention test, Seal Strength, Re-Eto and Re-dcm on GC etc.
EXECUTIVE, QUALITY CONTROL
Sahajanand Medical Technologies
04.2014 - 03.2021
- Prepared & reviewed various documentation including SOPs, test reports,test method ,maintained detailed records of all test results and logbooks
- Interpreted analytical results and prepared reports with conclusion
- Effectively carried out routine activities like inspection, set up of equipment, line clearance in accordance with GMP
- External and internal audits compliance
- Handling of analytical instruments like UV Cabinet, Ph meter, Conductivity meter,Polarimeter, Karl Fischer Titrator, Oxygen Content Analyzer, Tensile Tester, and Refractometer to perform raw material analysis.
SR. 0FFICER WET LAB, QC
Sahajanand Medical Technologies
12.2012 - 03.2014
JR.QUALITY CONTROL INSPECTOR
Sahjanand Medical Technologies
05.2011 - 12.2012
- Reviewed documents (BMR, checklists and batch reports) according to good documentation practice (GDP's)
- Reviewed the in-process test results, ensure the tests were performed according to the standard operating procedure (SOP) and those results are within the established specifications
- Activities such as logbooks issuance and archiving, periodic SOP review
- Analysis of raw material ,inprocess and finished product
- IPQC activity of production departments.Temperature and pressure monitoring of clean room
- Supported production needs by performing routine tasks using standard procedures and cGMP with complete records
- Review BMR(Batch manufacturing record), CR(Cleaning records
- Team up with Plant Operators for GDP.
Education
Bachelor of Science - Chemistry
Veer Naramd South Gujarat University
Surat,IndiaSkills
- Well versed with concepts of GMP,cGMP,GDP, GLP,FDA,ICH Guideline, ALCOA, USFDA& Health Canada
- Intermediate Knowledge of Microsoft office,SAP,LIMS,5S,WHIMS
- Handled HPLC(Shimadzu,Waters, Agilent)Empower-2&3,Labx Chemstation softwareGC(Perkin Elmer Clarus 580 Headspace Turbomatrix 40)IR, UV, KF,pH meter, Conductivity meter, viscometer, specific gravity bottle and manual Titration
- Individually and ability to work effectively in a team setting and achieve great success
- Good knowledge of day to day planning, execution and release of in-process samples,finished product,raw material and packing material
Timeline
QC, ANALYST 2
Germiphene Corporation
01.2023 - Current
QUALITY CONTROL CHEMIST
Bora Pharmaceutical
07.2022 - 01.2023
QUALITY CONTROL ANALYST
Genvion Corporation
06.2021 - 06.2022
EXECUTIVE, QUALITY CONTROL
Sahajanand Medical Technologies
04.2014 - 03.2021
SR. 0FFICER WET LAB, QC
Sahajanand Medical Technologies
12.2012 - 03.2014
JR.QUALITY CONTROL INSPECTOR
Sahjanand Medical Technologies
05.2011 - 12.2012
Bachelor of Science - Chemistry
Veer Naramd South Gujarat University
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