Thanmayee Thunga

Experience

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  Ramesh Hospitals

  Nov 2020 - Nov 2021

  Resident Care Associate - PharmD

  During my PharmD residency as a Resident Care Associate, my responsibilities included:- Patient Advising: Provided comprehensive counseling and guidance to patients regarding their medications, treatment plans, and lifestyle modifications to support better health outcomes.- Hospital Rotations: Collaborated closely with doctors during hospital rotations, gaining valuable exposure to multidisciplinary patient care and therapeutic decision-making processes.- Clinical Documentation: Accurately recorded patient information, medication history, and clinical notes in electronic health records (EHR), ensuring precise and up-to-date documentation.- Prescription Review: Carefully reviewed prescriptions to identify and prevent potential drug interactions, dosing errors, and contraindications, contributing to improved patient safety.- Drug Use Optimization: Focused on ensuring the safe and effective use of medications, achieving desired therapeutic outcomes while minimizing drug-related problems.- Therapeutic Management: Assisted in developing and implementing therapeutic strategies to address specific patient needs and optimize their medication therapy plans.This residency experience provided me with a solid foundation in patient care, clinical documentation, and medication management, enhancing my skills in pharmaceutical practice and interdisciplinary collaboration. Show less

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  Madhu Babu Hospitals

  Dec 2021 - Jul 2022

  Clinical Observership

  During my observership, my responsibilities included:- Patient Documentation: Recorded and maintained detailed patient visit notes within Electronic Medical Record (EMR) systems, ensuring accuracy and adherence to healthcare data standards and compliance guidelines.- Patient Interviews and Medical History Collection: Conducted patient interviews to collect comprehensive medical histories, vital signs, and chief complaints. Integrated collected information into clinical informatics platforms to support physician decision-making.- EHR Management and Record Updating: Assisted in updating and reviewing patient records within Electronic Health Records (EHRs), ensuring thorough documentation for the continuity of patient care and enhancing clinical workflows.- Patient Education and Preparation: Educated patients about their medications, treatment plans, and procedures while preparing them for examinations, contributing to the efficiency and effectiveness of medical evaluations.- Clinical Discussions and Learning: Engaged in clinical discussions with doctors, gaining valuable insights into healthcare management, patient-centered care, and the integration of informatics into clinical decision-making.This observership experience enriched my knowledge in clinical informatics, patient care, and effective healthcare management, reinforcing the importance of accurate documentation and patient-centered approaches in medical practice. Show less

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  Vignan Pharmacy College

  Aug 2022 - May 2023

  Assistant Professor

  During my tenure as an Assistant Professor of Hospital Pharmacy at Vignan Pharmacy College, my responsible included:Interdisciplinary Hospital Rotations: - Facilitated and coordinated hospital rotations for pharmacy students, collaborating with clinical departments and healthcare professionals to enhance students’ hands-on learning and patient care experiences.- Lecturing and Teaching: Delivered structured lectures on clinical pharmacy, pharmaceutical practices, and medication management, encouraging interactive discussions and fostering a collaborative learning environment.- Student Assessment and Evaluation: Graded assignments, tests, and projects using data-driven evaluation techniques to provide constructive feedback and ensure alignment with educational standards and objectives.- Patient Safety and Medication Monitoring: Supervised and monitored medication administration in healthcare settings, ensuring adherence to clinical protocols and patient safety guidelines.- Student Mentorship and Guidance: Advised students on their academic progression, career development, and personal goals, preparing them for advanced roles in the pharmaceutical and healthcare sectors.- Faculty Collaboration and Development: Actively participated in faculty meetings, contributing to curriculum development, accreditation processes, and initiatives to support the institution’s growth and continuous improvement.This opportunity not only solidified my expertise in clinical pharmacy but also sharpened my leadership, mentoring, and collaborative skills. It was an experience that profoundly shaped my professional life, laying a strong foundation for my career in both academic and healthcare settings. Show less

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  ScieGen Pharmaceuticals Inc

  May 2024 - Aug 2024

  Quality Control Chemist Trainee - Intern

  During my summer internship at ScieGen Pharmaceuticals, Inc., as a Trainee Quality Control Chemist, I gained practical experience in Quality Control (QC) laboratory practices and procedures. My responsibilities included:- Adherence to SOPs: Followed Standard Operating Procedures (SOPs) rigorously to maintain accuracy and compliance with QC laboratory standards.- Material Analysis: Conducted detailed analysis of raw materials, excipients, drug product containers, closures, in-process materials, packaging materials, labeling, and final drug products to verify they met required specifications.- Stability Testing: Performed stability testing to evaluate the shelf life and storage conditions of pharmaceutical products, ensuring product quality and safety throughout their intended lifespan.- Instrument Calibration: Calibrated various laboratory instruments regularly to maintain their accuracy and reliability in producing test results, emphasizing the need for precision and consistency.- Solution Preparation & Maintenance: Gained hands-on experience in preparing and standardizing volumetric solutions, reagents, and indicators. Maintained reference standards, working standards, and solutions for use in testing procedures.- Instrument Qualification: Executed Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of new instruments, ensuring their installation, operation, and performance were according to established standards.- Internal Audits: Actively participated in internal audits to confirm ongoing compliance with SOPs and regulatory standards, helping identify areas for improvement in laboratory processes.- Safety and Regulatory Training: Attended training sessions on safety protocols, Current Good Manufacturing Practices (cGMP), fire safety, emergency evacuation, and internal audit procedures to deepen my knowledge of safety and compliance requirements. Show less

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  ScieGen Pharmaceuticals Inc

  Feb 2025 - now

  Quality Control Trainee Scientist

  As a Quality Control Trainee Scientist my responsibilities are to ensure the highest standards of quality and compliance in pharmaceutical production through meticulous analysis and adherence to regulatory guidelines. My expertise spans from end-to-end quality control processes, including testing of packaging materials, raw materials, and drug products across in-process, finished, and stability stages.Key Contributions:- Conducting critical analysis of drug products, including moisture content determination using Karl Fischer (KF) titration and Tiamo software, ensuring accurate results for stability studies and product quality compliance.- Identifying and reporting Out-of-Specification (OOS), Out-of-Trend (OOT) results, and deviations, ensuring timely escalation to management and compliance with GMP standards.- Preparing and standardizing critical lab materials (volumetric solutions, reagents, indicators) while maintaining reference/working standards for accuracy.- Performing instrument calibration, verification, and validation, including execution of IQ/OQ/PQ protocols for new equipment.- Supporting internal audits and quality assurance initiatives, fostering a culture of continuous improvement and regulatory readiness.- Collaborating cross-functionally to optimize processes and uphold quality benchmarks in a cGMP-compliant environment. Show less