Nithej Talluri

• Enhanced research quality by providing thorough literature reviews and data analysis support.
• Assisted professors in development of course materials for improved student engagement and understanding.
• Managed administrative tasks such as grading, scheduling, and record-keeping to ensure smooth operations within academic departments.
• Mentored students with personalized guidance on academic progress, career goals, and professional development opportunities.
• Collaborated with faculty members on research projects, contributing to the advancement of knowledge in their respective fields.
• Contributed to departmental initiatives by participating in committees focused on curriculum development, accreditation processes, or program evaluations.
• Assisted in preparing, reviewing, and revision of departmental SOPs, methods, and worksheets under supervision of Dr. Isabelle Bichindaritz.
• Reviewed technical documents, analytical data, and reports generated by peers.
• Drafted and assembled reports, including data tables and appendices generated from raw data.
• Worked on website, maintain and fixing bugs with SQL and HTML and data base.
• Creating pages in website, managing social websites like Facebook, GitHub, twitter etc.
• Enhanced research quality by providing thorough literature reviews and data analysis support

• Improved patient safety by accurately reviewing and processing adverse event reports.
• Enhanced drug safety monitoring with thorough assessment of case data and identification of potential risks.
• Streamlined case management processes, ensuring timely submission of quality reports to regulatory authorities.
• Collaborated with cross-functional teams to develop risk mitigation strategies for drug products.
• Conducted comprehensive literature reviews to stay informed on new drug safety findings and trends.
• Boosted efficiency in handling individual case safety reports through meticulous tracking and organization.
• Utilized various databases effectively for efficient retrieval and analysis of drug safety data when needed.
• Communicated with internal or external contacts to resolve issues related to case processing.
• Responsible for case intake and acknowledging.
• Perform thorough duplicate check and registration of all types of reports Triage cases by standard criteria and business rules.
• Identify reports meeting minimum criteria (valid) and manage reports not meeting criteria(non-valid).
• Notify any potential SUSARs, urgent safety issues and event of special interest to client.
• Action on case closure and deletion of cases.
• Responsible for query reply management and version creation Responsible for follow-up requests.
• CASE PROCESSOR: Responsible for data entry of individual case safety reports into safety data base as per client conventions, guidelines, and SOPs.
• Full data entry including medical coding and safety narrative.
• Responsible for coding of events, drugs, laboratory tests according to appropriate dictionary (MedDRA, Company Product Dictionary, WHO-DD).
• Accountable for performing appropriate assessments (including seriousness, labeling and company causality).
• Sending queries to affiliates and responsible persons in case of any discrepancy in SAE forms.
• Adhering to SOPs and other controlled documents and regulatory requirements.
• Responsible for maintaining trackers related to team (leave tracker, productivity and quality tracker etc.).
• Review of literature articles and abstracts and identify case safety reports Ensures quality reviewing of literature searches and reports.
• Responsible for operational pharmacovigilance activities for assigned developmental and/ or marketed products.
• Whole Case Processing including Product coding, Event assessment, Seriousness criteria, narrative writing and conducting all required follow-up activities as required in SAPPHIRE, VEEVAVAULT and ARGUS safety database.
• Processing interventional study, non-interventional study/program, Perform daily Responsibilities in accordance with all applicable Standard Operating Procedures (SOPs), Conventions and client policies.

• TRAINER: Trained several sets of batches on the new PV intake database.

• Training and mentoring of new hires to ensure highest quality

• Finding the quality error of the team and reiterating the team each error in QC Huddle session as SME.

• Enhanced product quality by conducting thorough analyses and implementing corrective actions.
• Improved overall production efficiency by identifying and resolving quality control issues.
• Reduced customer complaints with consistent monitoring of products for adherence to company standards.
• Streamlined processes, implementing rigorous testing protocols to ensure product reliability.
• Developed comprehensive documentation, maintaining accurate records of quality control results and actions taken.
• Maintained safe working environment, adhering to safety regulations and proper handling of hazardous materials.
• Conducted root cause analysis for recurring issues, developing long-term solutions to prevent recurrence.
• Ensured regulatory compliance by staying updated on industry standards and government regulations affecting product quality.
• Evaluated risks associated with potential changes in processes or materials, mitigating negative impacts on final products.
• Adhered to safety and clean area procedures to comply with agency and regulatory mandates.
• Reviewed and validated quality requirements for manufacturing planning, supplier purchase orders, and engineering specifications to meet contract compliance regulations.
• Determined root cause of deviations and non-conforming results and implemented appropriate corrective and preventive actions throughout product development process.
• Inspected incoming products for adherence to labeling laws and company quality standards.
• Instructed vendors or contractors on quality guidelines, safety procedures, testing procedures and ways to eliminate deficiencies.
• Analyzed quality and performance data to support operational decision-making.
• Recorded findings of inspection process, collaborating with quality team to implement corrective actions.
• Created and collaborated in implementation and maintenance of customer complaint log.
• Consulted manuals and process documents to investigate malfunctions.
• Developed and maintained quality assurance procedure documentation.
• Developed training materials, SOPs and work instructions to supplement new team member onboarding.
• Reported problems and concerns to management.
• Led process improvement projects to help operations meet and exceed quality standards and reduce costs.
• Liaised with vendors and end-users to uncover system optimization opportunities.
• Reviewed production processes and identified potential quality issues.
• Monitored testing procedures and verified performance of tests according to established item specifications and protocol.
• Recorded and organized test data for report generation and analysis.
• Performed routine maintenance and calibration on testing equipment.
• Developed and implemented procedures to meet product quality standards.
• Completed supporting documentation for testing procedures, data capture forms, equipment logbooks and inventory forms.
• Conducted investigations into questionable test results.
• Assessed products or services to evaluate conformance with quality standards.
• Liaised between quality control and other departments and contractors, providing project updates and consultation.
• Drafted technical documents such as deviation reports, testing protocol and trend analyses.
• Created testing protocols to be used across product lines.

• Enhanced intern productivity by assisting with project coordination and providing ongoing support.
• Streamlined office processes for improved efficiency and time management through regular organization and filing.
• Contributed to positive team environment by collaborating with fellow interns on group projects and presentations.
• Supported staff members in their daily tasks, reducing workload burden and allowing for increased focus on higher-priority assignments.
• Case study.
• Detailed study of Criminal case of victim.
• Analysis of techniques used to solve Criminal case.
• Performing various tests on samples extracted from viscera.
• Writing report on experiment and tests conducted on victim viscera.
• Extraction of Viscera and give markings on it as per related case.
• DNA Tests are performed to identify genetic parental of child.
• Developing and extracting Blood strains and other body Fluids from fabric collected as Evidence.
• Matching body fluids with victim, collected at crime spot.
• Analysis of techniques used to solve case.
• Performing various tests on samples extracted.
• Writing report on experiment and tests conducted on samples.