Senior Scientist ADME Job at Syngene | Apply Now for Pharma Research Job
If you are looking for a Senior Scientist ADME Job in the pharmaceutical research sector, this opportunity at Syngene International Ltd. could be the perfect next step in your career. This Pharma Job in Hyderabad focuses on advanced ADME and DMPK research, supporting drug discovery and development for small molecules. Candidates with strong expertise in in-vitro metabolism assays and ADME studies can contribute to cutting-edge pharmaceutical research while working with global industry leaders.
- Job Title: Senior Scientist – ADME
- Job Location: Hyderabad
About the Company
Syngene careers is an innovation-focused global discovery, development, and manufacturing organization. Incorporated in 1993, the company provides integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world.
Syngene’s clientele includes global leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. The organization is driven by a strong culture of innovation powered by a team of over 4,240 scientists who collaborate with global clients to solve scientific challenges, improve R&D productivity, accelerate time to market, and reduce the cost of innovation.
Job Description
- Support the ADME in-vitro metabolism team in drug discovery and development for small molecules.
- Conduct liver microsome and CYP inhibition assays for ADME studies.
- Operate liquid handling systems and automation platforms.
- Maintain accurate documentation of laboratory activities and experiments.
- Follow safety rules and maintain proper lab housekeeping standards.
- Handle high-volume Wave 1 ADME assays while managing multiple projects within timelines.
Key Responsibilities
- Plan and execute in vitro metabolism assays with extensive expertise.
- Design and perform in vitro metabolism studies, including single-point inhibition, reversible CYP IC₅₀ inhibition, and TDI-IC₅₀ shift assays using human liver microsomes.
- Preparation of SOP’s and EOPs.
- Reporting of executed studies without any noncompliance.
- Reporting of study results clearly in the cross-functional scientific meetings.
- Follow environment, health, and safety (EHS) requirements at all times in the workplace, ensuring individual and lab/plant safety.
- Ensure environment, health, and safety (EHS) measures are imparted via training and adhered to within the team.
Qualification
- M Pharm. in any pharmaceutical science or M Sc. in biological science.
Technical/functional Skills
- Comprehensive understanding of in vitro ADME assays and technical expertise in troubleshooting the assays.
- Good, demonstrated knowledge in software such as Microsoft Excel and GraphPad Prism.
- Demonstrated cross-functional leadership capabilities.
- Experience with automation is desirable.
Experience
- M Pharm. in pharmaceutical sciences or M SC in biological science with foundational years of Industrial experience in DMPK/ADME research.
Behavioral Skills
- Demonstrate ability to be a team player.
- Commitment to deliver the study reports within the agreed timelines.
- Adaptability to changes in the dynamic lab environment.
- Communicate confidently with colleagues and collaborators in meetings and presentations of study reports and evidence of publications in peer-reviewed journals.
