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2.0 - 7.0 years
10 - 11 Lacs
Hyderabad
Work from Office
Your key responsibilities will include conducting In Vitro ADME studies This involves reading and understanding various in vitro ADME protocols, as well as performing in vitro stability experiments for new chemical entities in liver microsomes, plasma, and other relevant matrices You will also conduct specific in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations, CYP phenotyping, and solubility determinations in various cell lines In addition to in vitro ADME studies, you will be involved in bioanalysis activities This includes developing and validating LC-MS/MS and HPLC-UV/PDA methods, conducting bioanalytical QC, and handling bioanalytical method development for various matrices with a focus on in vitro samples Experience in developing LC-MS/MS methods for biochemical and cell-based screening of NCEs is a plus You will also be responsible for general LC-MS/MS and HPLC maintenance and troubleshooting tasks Furthermore, as part of your role, you will be required to analyze data, generate reports, and share them with the line manager This involves understanding the quality of bioanalytical data, conducting data analysis using software like Phoenix WinNonLin, calculating in vitro results/parameters using Excel spreadsheets, and generating reports in Excel, Word, and PowerPoint formats You will also be responsible for generating reports in both GLP and non-GLP formats based on the requirements
Posted 4 days ago
2.0 - 7.0 years
10 - 11 Lacs
Hyderabad
Work from Office
Your key responsibilities will include conducting In Vitro ADME studies. This involves reading and understanding various in vitro ADME protocols, as well as performing in vitro stability experiments for new chemical entities in liver microsomes, plasma, and other relevant matrices. You will also conduct specific in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations, CYP phenotyping, and solubility determinations in various cell lines. In addition to in vitro ADME studies, you will be involved in bioanalysis activities. This includes developing and validating LC-MS/MS and HPLC-UV/PDA methods, conducting bioanalytical QC, and handling bioanalytical method development for various matrices with a focus on in vitro samples. Experience in developing LC-MS/MS methods for biochemical and cell-based screening of NCEs is a plus. You will also be responsible for general LC-MS/MS and HPLC maintenance and troubleshooting tasks. Furthermore, as part of your role, you will be required to analyze data, generate reports, and share them with the line manager. This involves understanding the quality of bioanalytical data, conducting data analysis using software like Phoenix WinNonLin, calculating in vitro results/parameters using Excel spreadsheets, and generating reports in Excel, Word, and PowerPoint formats. You will also be responsible for generating reports in both GLP and non-GLP formats based on the requirements.
Posted 4 days ago
10.0 - 20.0 years
27 - 42 Lacs
Vadodara
Work from Office
Familiarity with multiple and diverse bioassay techniques for study of enzymes, kinases, GPCR’s, RNA binding proteins, epigenetic targets etc. Required Candidate profile Oversee in vitro screening experiments and generate reports in a timely manner Propose new ideas, conduct and assist in target evaluations & due diligences
Posted 2 months ago
2.0 - 4.0 years
4 - 5 Lacs
Guwahati
Work from Office
Marketing mapping Understand client needs & develop revenue pipeline in alignment with the BD strategy Identifying new biz opportunities & capitalize Negotiate & close contracts/agreements as per policy Farming existing clients & ensuring growth Required Candidate profile Manage & develop customer relationship & customer satisfaction Client retention Responsible for cross dept. collaboration across Co for smooth operations Responsible for sales for the assigned area
Posted 2 months ago
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