Rekha Vadloori
Quality Assurance / Quality Control Associate (Entry-level) • Hyderabad, Telangana • H************************@gmail.com • +91*******924 • drivetube.ai/•••••
Career Objective
Quality Assurance / Quality Control Associate with 0 years of experience seeking an entry-level position in pharmaceutical QA, QC or production to apply B.Pharm training in formulation development, analytical testing, GMP-compliant documentation, and continuous process improvement.
Education
Jyothishmathi Institute of Pharmaceutical Science, Thimmapur, Karimnagar
Bachelor of Pharmacy (B.Pharm), CGPA: 8.8 • Thimmapur, Karimnagar, Telangana • 2020 – 2024
T S Model School & Jr.College, Rahimkanpet, Rajanna Siricilla
Higher Secondary (Intermediate), CGPA: 9.0 • Rahimkanpet, Rajanna Siricilla, Telangana • 2018 – 2020
Z P High School, Ellanthakunta, Karimnagar
Secondary School Certificate (SSC), CGPA: 9.0 • Ellanthakunta, Karimnagar, Telangana • 2018 – 2018
Technical Skills
Testing: Quality Assurance QA,Quality Control QC,Good Manufacturing Practices GMP,Standard Operating Procedures SOP adherence,Batch documentation review
Data and Analytics: MS Office Word, Excel,Excel data analysis,Laboratory equipment handling,Experimental data recording and interpretation,Report writing,Documentation and regulatory record keeping
Pharmaceutical Skills: Oral thin film formulation,Fast dissolving film development,Pharmaceutical formulation development,Drug delivery systems,Excipient selection,Dose uniformity testing
Laboratory Techniques: Disintegration testing,Dissolution and drug release studies,Thickness measurement,Sample preparation,In-process quality checks
Professional Skills: Attention to detail,Teamwork and communication,Adaptability
Projects
Fast Dissolving Oral Film of Domperidone | 2024
Tools Used: Oral thin film formulation, Disintegration testing, Dissolution and drug release studies, Thickness measurement, Experimental data recording and interpretation
- Formulated domperidone fast dissolving oral films using established pharmaceutical techniques to produce uniform, handleable film strips suitable for oral administration.
- Designed and executed evaluation tests including thickness measurement, disintegration time assessment, and drug release studies to assess performance of developed formulations.
- Prepared samples and carried out systematic experimental data recording, then analyzed and interpreted results to compare formulation batches and identify optimal composition.
- Documented procedures, observations, and findings in lab reports; summarized formulation insights relevant to stability and patient acceptability for academic evaluation.
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