Role Overview
Jubilant Biosys is hiring a mid-level QC and Research Assistant. This is a full-time role in IN. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
As an In Vitro ADME Studies expert, your role involves conducting various in vitro ADME experiments and bioanalysis to support drug discovery processes. Your key responsibilities include:
- Reading and understanding various in vitro ADME protocols.
- Conducting in vitro stability experiments for new chemical entities, including liver microsomes, plasma, and other relevant matrices.
- Performing in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations in relevant cell lines, CYP phenotyping, and solubility determinations.
- Developing and validating LC-MS/MS and HPLC-UV/PDA methods for in vitro sample analysis.
- Extracting data from instruments, conducting bioanalytical QC, and sharing reports with DMPK stakeholders.
- Analyzing bioanalytical data, calculating in vitro results using Excel, and generating reports in Excel, Word, and PowerPoint format.
- Maintaining and troubleshooting general LC-MS/MS and HPLC instruments.
Additional details of the company were not provided in the job description.
Qualifications required for this role include:
- Education: M.Sc / M.Pharm
- Experience: 2-6 years in a drug discovery industry/CRO in the DMPK department
Your expertise in in vitro ADME studies and bioanalysis will be crucial in contributing to the drug discovery processes and supporting the DMPK department's goals. As an In Vitro ADME Studies expert, your role involves conducting various in vitro ADME experiments and bioanalysis to support drug discovery processes. Your key responsibilities include:
- Reading and understanding various in vitro ADME protocols.
- Conducting in vitro stability experiments for new chemical entities, including liver microsomes, plasma, and other relevant matrices.
- Performing in vitro ADME experiments such as logP, logD, pKa measurements, CYP induction and inhibition assays, permeability determinations in relevant cell lines, CYP phenotyping, and solubility determinations.
- Developing and validating LC-MS/MS and HPLC-UV/PDA methods for in vitro sample analysis.
- Extracting data from instruments, conducting bioanalytical QC, and sharing reports with DMPK stakeholders.
- Analyzing bioanalytical data, calculating in vitro results using Excel, and generating reports in Excel, Word, and PowerPoint format.
- Maintaining and troubleshooting general LC-MS/MS and HPLC instruments.
Additional details of the company were not provided in the job description.
Qualifications required for this role include:
- Education: M.Sc / M.Pharm
- Experience: 2-6 years in a drug discovery industry/CRO in the DMPK department
Your expertise in in vitro ADME studies and bioanalysis will be crucial in contributing to the drug discovery processes and supporting the DMPK department's goals.
Frequently Asked Questions
How do I apply for the QC and Research Assistant position at Jubilant Biosys?
Use the Apply button above to submit your application directly to Jubilant Biosys. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the QC and Research Assistant position at Jubilant Biosys located?
This position is based in IN. Jubilant Biosys has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a QC and Research Assistant at Jubilant Biosys earn?
Jubilant Biosys has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the QC and Research Assistant role at Jubilant Biosys posted?
This role was posted on April 17, 2026 (67 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
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