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Xogene combines regulatory expertise with advanced technology to automate complex processes in clinical trial disclosure. As trusted experts with comprehensive knowledge of global regulatory frameworks, we deliver efficient data transformation and regulatory compliance for our clients, streamlining workflows through our AI and agentic networking capabilities. We're committed to leveraging technological solutions to advance clinical trial transparency.

Responsible for ensuring operating state of cGMP compliance in Solution/Emulsion preparation, vial/ampoule washing, Depyrogenation, Filling, Capping and Collection operations.

Adverse Event Reporting Officers must have strong organizational, communication and problem-solving skills. In addition, they are responsible for daily source document quality reviews. Adverse Event Reporting Officer report directly to Team Lead, AERO.

Master / Integrated Masters in Organic / Pharmaceutical / General Chemistry with experience in organic synthesis. CSIR-National Chemical Laboratory, Pune

Institute of Bioresources and Sustainable Development Fellowships | 41 fellowships in different research

M.Sc./ B.E./ B.Tech. or equivalent degree with at least 55% marks and one publication in Science Citation Indexed Journal and should have completed at least two years of post-M.Sc./ B.E./ B.Tech. Human Resource Development (HRD) Group of COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (CSIR), New Delhi

Smart Diagnostics of Rotating Machinery: A Digital Twin Approach for Industries using Physics-Based Simulation and AI/ML. IIT Bombay

Diploma in Ayurvedic Pharmacy from any recognized University/ institution or Board or faculty of Indian System of Medicine established by law in India or recognized by the Govt. Shri Krishna AYUSH University, Kurukshetra

The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs)