Roles & Responsibilities
• Perform routine analytical testing of in-process and isolated samples
• Analyze early intermediates and APIs using chromatographic and wet analytical techniques
• Execute method qualification and support instrument calibration activities
• Maintain accurate and compliant documentation using Electronic Lab Notebooks (ELN)
• Ensure adherence to GxP guidelines and quality standards
• Handle general laboratory responsibilities and support ongoing Analytical R&D activities
• Contribute to API development and chemical research programs
Qualification
• M.Pharm (Pharmaceutical Analysis / Analytical Chemistry preferred)
Experience
• Relevant experience in Analytical R&D within pharmaceutical or CRO/CRDMO environments preferred
Skills
• Strong theoretical and practical knowledge of analytical chemistry
• Hands-on experience with chromatographic techniques
• Understanding of method qualification and instrument calibration
• Knowledge of GxP documentation and compliance standards
• Proficiency in MS Office tools (Word, Excel, PowerPoint)
• Strong communication, documentation, and teamwork skills
• High attention to detail with a proactive and ethical work approach
• Willingness to work in shifts, if required
About the Organisation
Syngene International Ltd. is a leading global Contract Research, Development, and Manufacturing Organization (CRDMO) supporting pharmaceutical and biotechnology companies worldwide. Known for its strong scientific capabilities and innovation-driven culture, Syngene offers professionals exposure to cutting-edge API development, analytical research, and global drug discovery programs.
Unlock refined AI insights.