Manasa Vutukuru
Belfast
Summary
With a Bachelor’s degree in Pharmacy and a Master’s in Pharmaceutical Analysis, I bring two years of GMP experience through a placement program as an Associate Scientist and a one-year internship in Quality Control. I possess expertise in regulatory compliance, GMP/GLP standards, and advanced techniques such as HPLC, FTIR, and UV/Vis spectrophotometry. Proficient in LIMS, SAP, and regulatory documentation, I successfully improved report turnaround time by 20% through optimized data management processes, ensuring high-quality regulatory submissions and compliance.
Overview
3
3
years of professional experience
Work History
Associate Scientist
Sygnature Discovery
Nottingham
09.2023 - 06.2024
- Conducted routine analysis of pharmaceutical products using techniques such as HPLC, UPLC, FTIR, UV, and wet chemistry techniques.
- Accurately recorded data in the documentation and reported any OOS, OOT, and OOE results to management. Identified deviations and communicated them for resolution.
- Utilized LIMS for sample logging, management, and data entry, ensuring high standards of accuracy.
- Conducted regular inventory checks to ensure adequate supplies of consumables and solvents. Reordered items as necessary to maintain laboratory operations.
- Maintained detailed, clear, and concise records of all analytical activities and reviewed and compiled data into reports to support regulatory submissions.
- Ensured data quality and integrity while adhering to GMP and cGMP standards.
- Understanding of SOPs, ICH, and ISO guidelines. Participated in safety audits and adhered to COSHH and EHS standards.
- Contributed to equipment calibration and preventive maintenance schedules.
- Collaborated with cross-functional teams to resolve quality issues and improve analytical processes.
QC Intern
Optimus Drugs Pvt Limited
Hyderabad
06.2021 - 06.2022
- Analyzed 500+ samples for quality benchmarks monthly, using HPLC and wet chemistry techniques.
- Prepared Certificates of Analysis (CoAs) and batch records in compliance with CDSCO and Indian Pharmacopoeia (IP) standards.
- Collaborated with R&D and production teams to resolve quality issues and improve product formulations.
- Supported the calibration and preventive maintenance of laboratory instruments to ensure accuracy.
- Conducted cleanliness checks and monitored environmental conditions to ensure compliance with regulatory standards.
Education
Masters in Pharmaceutical Analysis With Industrial Placement - Chemistry and Chemical Engineering
Queen's University Belfast
Belfast, United Kingdom08-2024
Bachelor of Pharmacy - Pharmaceutical Science
Osmania University
Hyderabad, India07-2021
Skills
- HPLC, UPLC, UV, FTIR analysis, and wet chemistry techniques (pH, conductivity, titrations, viscosity)
- LIMS , SAP, Trackwise , MS Ensuite ( MS Word, Excel and Power Point
- Data Interpretation
- Troubleshooting
- Instrument Calibration
- Date Integrity, GDP (ALOVA) and GMP Compliance
- OOS, OOT, lab incidents & investigations
- COSHH Knowledge
- Knowledge of SOP, ICH, ISO standards, and analytical method validation & transfer principles
Languages
Telugu
First Language
English
Proficient (C2)
C2
Hindi
Proficient (C2)
C2
Competencies
- Communication skills
- Analytical Thinker
- Attention to Detail
- Team Work
Accomplishments
- Testing Accuracy: Achieved a 40% improvement in testing accuracy by implementing advanced automation techniques, significantly enhancing data reliability in a GMP setting.
- Reporting Efficiency: Streamlined data management processes, resulting in a 20% reduction in report turnaround time at Sygnature Discovery, facilitating timely regulatory submissions.
Timeline
Associate Scientist
Sygnature Discovery
09.2023 - 06.2024
QC Intern
Optimus Drugs Pvt Limited
06.2021 - 06.2022
Masters in Pharmaceutical Analysis With Industrial Placement - Chemistry and Chemical Engineering
Queen's University Belfast
Bachelor of Pharmacy - Pharmaceutical Science
Osmania University
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