Job Summary

• Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
• Responsibilities include document control in a GLP system, ensuring compliance with regulatory guidelines, and managing laboratory equipment.
• The role supports clinical sample management, including shipment tracking and sponsor communication, while adhering to safety and quality standards.

Matching Summary

Skills & Requirements

Key Requirements

• Entry level lateral from science background
• Ph.D. in Biotechnology
• Vector design knowledge
• Protein expression knowledge
• Cell line engineering knowledge

Work Rights