Research Associate
Key responsibility:
- Organized and conducted different stability and verification studies for Astute medical device development.
- Gathered, arranged, and corrected research data to create representative graphs and charts highlighting results for FDA submission.
- Requested and acquired chemicals for study.
- Worked collaborative with other product development team to meet project deadlines and goals.
- Followed guidelines and protocols to maintain quality of product testing.
- Substantial pipetting and aliquoting human specimen.
- Worked with spreadsheet and Excel Analyse-it to outline data.
- Validated and verified data with principal scientist for data accuracy.
- Performed preventative maintenance of laboratory equipments.
- Executed validation activities when needed.
- Conduct calibration of meter, an Astute device used for data collection.
- Mediated with quality assurance team for FDA submission.
- Maintained laboratory notebooks with protocol,testing,data collection, report and analysis using GDPs.
- Identified and trouble shoot issues when needed.
Additional Responsibilities :
- worked in sample bank to keep a track of patient samples.
- Aliquots samples mainly urine sample for PD testing.
- Prepared and shipped of patient samples to different sites.
- Worked with software used for ELISA and assay plates.
- Inspected lab equipment to ensure safety on monthly basis following EH&S requirements.
- Provided training of Astute protocols and procedures to newly appointed RAs.
- Helped software developer to test different software used in Astute medical.