Job Overview
-
Date PostedSeptember 28, 2022
-
Location (State / UT)
-
Expiration date--
-
Experience2 Years, 6 Years
-
GenderAny
-
Desired QualificationMaster’s Degree
Job Description
Roles and Responsibilities:
- Perform in-vitro ADME studies like solubility, metabolic stability, PAMPA/Caco-2 permeability, and plasma protein binding
- To perform in vitro DDI studies like CYP Inhibition, and PXR activation and integrate the data as per regulatory guidelines for in vitro DDI
- Prepare study documents and reports in compliance with regulatory filing
- Support performing PK and immunogenicity assays for new biologics
Desired Candidate Profile:
2-3 years of work experience in performing in vitro DMPK assays in new drug discovery research with some exposure to ELISA assays
- Must have a good understanding of drug metabolism, drug transport, drug-drug interactions, enzymology, and pharmacokinetics principles Hand-on experience performing high throughput in vitro ADME and DDI assays.
- Ability to analyze the ADME data and prepare reports
- Should know the use of Graph pad prism or other appropriate software
- Should be familiar with regulatory guidance o in vitro DDI
- Hand experience performing PK and immunogenicity assays would be an advantage
Perks and Benefits
- 5-day working
- AC bus for transportation from Baroda
- Excellent work culture
Qualification: M.Pharma