Haryana

Post Graduate (M.Sc.) in Biochemistry / Biotechnology / Microbiology / Life Sciences / applied science with First Division. Central University of Haryana, Jant-Pali, Mahendergarh, Haryana

Coordinate with cross-functional teams, including Clinical, Quality, and Manufacturing, to gather necessary regulatory documentation.

Develop and execute regulatory strategies, providing leadership and guidance on pharmaceutical regulatory requirements across India and South Asia to support product registrations, market access, launches, lifecycle management, and post-market compliance.

The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The role is critical to meet planned Site Ready dates

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.

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

Bachelor degree in Pharmacy from a recognized institute. Or Diploma in Pharmacy. The candidate should be registered in State Pharmacy Council.

PhD in Biotechnology / Biochemistry Microbiology / Plant Biology / Bioengineering / Agricultural Microbiology / Life Sciences from a recognized university. Should have strong experience in design and development of research experiments related to plant physiology. Regional Centre for Biotechnology

Looking for motivated and detail-oriented candidates to join DDReg Pharma as RA Trainees. This role provides an opportunity for freshers to build their career in the Regulatory Affairs domain while gaining practical exposure to regulatory documentation, submissions, dossier preparation, and regulatory guidelines.