5 years
3 - 8 Lacs
Posted:-1 days ago|
Platform:
Work from Office
Full Time
Qualifications required: Bachelors /Masters (2-6 Years of experience in Bioanalytical Department only) Role and responsibility: 1. To work on the method development / validation / study sample analysis using HPLC, LC/MS/MS techniques as per principles of GLP, SOPs and approved protocols. 2. To plan and monitor the laboratory work involving the various processing techniques, analytical methods and standard operating procedures (SOPs) and complying with the principles of Good Laboratory Practices (GLP) as well as approved protocols to ensure the quality, integrity and reliability of the results. 3. To establish quality control program and safety of the staff and to establish corresponding corrective actions. 4. To review the raw data forms and chromatographic data sheets 5. To electronically transfer the data duly checked with the raw data and chromatograms to Pharmacokinetics department for PK analysis. 6. Review of Method SOPs, bio-analytical reports of Method Validation and Studies. 7. Review and/or approval of operational SOPS and Method SOPs. 8. Training of personnel. 9. Responding to queries from Sponsor and/or regulatory authorities.
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