Posted:2 weeks ago|
Platform:
Work from Office
Full Time
1. Proper maintenance of LC-MS/MS/ HPLC/ UPLC and their records of calibration.
2. To develop and validate Bio-analytical methods.
3. To process and analyse biological samples for drug/metabolite concentrations
4. To compile raw data and record laboratory note books/logbooks
5. To maintain equipment logbooks
6. To assist Lab Manager in data analysis and compilation of reports
7. Proper operation and routine maintenance of laboratory equipment in Bio analytical department
8. Responsible for laboratory instruments like PH meter, analytical balance, micro pipettes, etc.
9. Recording and reviewing of all raw data, method SOPs method validation reports and bio analytical reports of the studies.
10. Online Documentation, raw data recording, chromatographic data printing and method note book checking
11 . Review and authorize IQ/OQ/PQ documents
12. Approve/authorize validation, analytical and other reports in absence of the head-BA.
1. Hands-on expertise in developing and validating bioanalytical methods in accordance with regulatory guidelines (e.g., FDA, EMA, ICH).
3. Demonstrated ability to lead teams, coordinate with cross-functional departments, and guide junior scientists.
4. Meticulous in maintaining accurate and audit-ready documentation as per GLP and regulatory standards.
BDR Pharmaceuticals
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