NIRAV CHOVATIYA
London,United Kingdom
Summary
Quality-focused QC Analyst experienced in analysing finished products, raw materials, and stability products to ensure compliance with quality standards. Demonstrated ability to work efficiently in busy laboratories, meeting critical timelines while maintaining attention to detail and proficiency in various physical and chemical techniques. Committed to contributing to analytical laboratory through strong communication skills and hands-on experience with equipment such as HPLC, TLC, FTIR, UV Spectrometer, and KF titrator.
Overview
4
4
years of professional experience
Work History
Quality Control Analyst
ARC Pharma
, United Kingdom
07.2025 - Current
- Chromatography techniques, including HPLC (high performance liquid chromatography) analysis for a variety of tests such as assay, dissolution, troubleshooting of HPLC instruments, and interpretation of chromatographic data.
- Expertise in using various spectroscopies, such as FTIR, UV-Vis spectrophotometer, and KF titrator.
- Implemented lab health and safety requirements alongside GMP principles to ensure compliance and safety standards.
- Supported comparative AMT from various clients by evaluating method performance parameters to enhance data reliability.
- Handled chemicals and conducted COSHH risk assessments while maintaining and calibrating lab equipment and ensuring compliance with 5S housekeeping standards.
- IT skills such as the use of MS Office, including MS Word, MS Excel, and software like Lab Solution, SDMS, and LIMS.
Quality Control Analyst
Bristol Laboratories Ltd.
, United Kingdom
09.2022 - 07.2025
- Analysed finished products, raw materials, stability samples and cleaning validation in Quality Control department, ensuring compliance with SOP and GLP, and documenting results in real-time through LIMS following ALCOA principles.
- Developed and validated analytical methods to enhance quality control processes.
- Prepared report on analytical study and supported investigations of OOS, OOT, lab incidents, and deviations through QMS with appropriate CAPAs.
Education
Master of Science - Drug Discovery and Development
University of Central Lancashire
Preston, United Kingdom01-2024
Bachelor of Science - Chemistry
Sir P.T. Sarvajanik College of Science
Surat, India01-2019
Skills
- HPLC analysis
- UV spectrophotometry
- Analytical testing
- Stability testing
- Instrumentation troubleshooting
- Finished goods inspections
- Wet chemistry techniques
- GMP principles
- COSHH Assessments
- Root Cause Analysis
- Statistical analysis techniques
REFERENCES
- References available upone request.
Timeline
Quality Control Analyst
ARC Pharma
07.2025 - Current
Quality Control Analyst
Bristol Laboratories Ltd.
09.2022 - 07.2025
Master of Science - Drug Discovery and Development
University of Central Lancashire
Bachelor of Science - Chemistry
Sir P.T. Sarvajanik College of Science