Dynamic Researcher with hands-on experience in in-vitro and in-vivo research,mammalian cell culture, talent for navigating challenges. Brings strong problem-solving skills and proactive approach to new tasks. Known for adaptability, creativity, and results-oriented mindset. Committed to making meaningful contributions and advancing organizational goals.
Overview
13
13
years of professional experience
1
1
Certification
Work History
Lab Manager
McMaster University
02.2024 - Current
Oversee the collection, entry, verification, management, analysis, and reporting of data
Use statistical software to analyze data and interpret results
Design and maintain databases, data collection forms, error checking methods and related programs for efficient collection, analysis, and reporting
Modify and reconfigure databases to ensure the optimal storage of data and minimize data entry complexities
Troubleshoot moderately complex computer problems
Write data management and operations documentation for the project
Liaise between the project centre and remote project sites and personnel
Conduct structured project participant interviews
Ensure that the relevant research methodology is applied and all research material is handled in accordance with established protocols, policies, and procedures
Develop presentations and present information and training sessions to project personnel and project participants
Keep project participants informed of project progress through regular reports and newsletters
Gather and compile information and data required for the preparation of scientific papers, abstracts, and graphs
Conduct literature searches
Oversee the extraction and compilation of data required for reports and disseminate data to research groups and collaborating partners
Implement and maintain the research project budget
Create financial projections and make adjustments to the research project budget throughout the fiscal year
Exercise appropriate budget controls, monitor, and reconcile accounts
Write a variety of letters and memos
Participate in research project meetings and propose recommendations for procedure modifications and development in the areas of data management, quality control, and assurance
Write, update, and archive data management and quality assurance conventions
Respond to inquiries received from project personnel regarding relevant project issues and procedures.
Senior Research Associate
Triumvira Immunologics, Inc.
03.2022 - 12.2023
Manage mouse colonies, overseeing breeding and genotyping of transgenic animals
Conduct routine technical procedures in rodents, administering test articles through various routes (intravenous, intramuscular, etc.)
Monitor animal health, perform anesthesia, and conduct blood sampling
Demonstrate impeccable tissue culture techniques, including primary cell culture and cell isolation
Execute euthanasia, tissue collection, and the collection of lymphocytes and splenocytes, along with necropsy procedures
Coordinate the shipment of samples and their analysis at local laboratories
Accurately prepare dosing materials, involving calculations and dilutions
Adhere to study protocols, animal use protocols, and Standard Operating Procedures (SOPs)
Maintain detailed lab records, whether in paper or electronic formats
Perform various facility-related procedures, including surgical instrument preparation, record-keeping, inventory maintenance, document review, and database management.
Immunochemistry Quality control Reviewer( support scientific)
Charles River Laboratories
03.2021 - 03.2022
Manage electronic document life cycle, including creation, revision, archival, retention, and withdrawal/retirement
Oversee Document Change Control to ensure compliance with regulatory requirements and site practices
Issue GxP documents (batch records, logbooks, worksheets) for QC, clinical, and commercial manufacturing
Maintain Procedural Document Binders or electronic equivalents
Scan and file executed documents physically and electronically, organizing document control file rooms
Ensure secure and retrievable storage of GMP records, adhering to defined retention periods
Support periodic document reviews and maintain alignment with the documented quality system and regulatory requirements
Represent the department in cross-functional project teams
Provide support during regulatory audits and inspections
Perform additional assigned duties and responsibilities
Collaborate with the Scientist to compile and assemble study deliverables in an audit ready state for submission to the Quality Assurance department (QA) and answer QA findings
Preparing or revision of the study summary (e.g MQS, MVS) when required
Perform all other related duties assigned.
Toxicology Research
ITR Laboratories Canada Inc.
03.2019 - 03.2021
Leads and completes scheduled work activities such as preventative maintenance, corrective maintenance, calibrations and troubleshooting
Administration of substances (IV, gavage, infusion, subcutaneous, IP, inhalation)
Collection of biological samples (urine, blood, feces) and various parameters (observations, body weight, food consumption, vital signs)
Assure the wellbeing and welfare of the animals (husbandry)
Record meticulously study raw data and perform study activities, following the study plan, the established SOPs and the GLP regulation
Make recommendations for the improvements in the study to the manager
Review the daily schedule day to day basis.
Doctoral Researcher
JNTU Anantapur
11.2011 - 02.2019
Set up and conduct biological, microbiological and biochemical tests and laboratory analyses in support of research and quality control in food production, sanitation, pharmaceutical production, biotechnology and other fields
Applied methods and techniques such as microscopy, histochemistry, chromatography, electrophoresis and spectroscopy
Performed experimental procedures in agriculture, plant breeding, animal husbandry, biology and biomedical research
Conducted field research and surveys to collect data and samples of water, soil, and plant and animal populations
Growing microbe cultures
Analyse data and prepare reports
Investigating results for microbiological data
Using computers and a wide variety of laboratory instruments to carry out experiments
Ensuring products and processes comply with all relevant SOP's, principles and regulations
Involved in the production, testing and packing of vials
Writing up research findings and then producing conclusive reports.