September 2025

Graduate in Pharmacy or Life Sciences. 2 years in the field of Regulatory Affairs/ Quality Assurance/ Quality control/ Manufacturing/ Analytical Development/ R&D.

This role involves researching, writing, and adapting scientific information into accurate, compliant, and engaging materials for healthcare professionals, patients, and other stakeholders.

Candidate should be B.Sc./ M.Sc./ B.Pharma/ M.Pharma with 3 to 6 years of experience working with Pharma Industry

MBA / B Pharma / M Pharma - Life Sciences academic background or B Tech / BE / M Tech / ME - Engineering academic background.

Hands-on experience in facing regulatory inspections. Strong knowledge of Good Manufacturing Practices

Act as a point of communication between the project personnel and the sponsor in order to resolve queries related to project activities

Conducted routine and on-demand literature search activities for the Alcon Knowledge Center, supporting internal stakeholders by refining search strategies to enhance the relevance and quality of retrieved publications.

Amneal Pharmaceuticals, Inc. announced the submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for a proposed biosimilar to XOLAIR

The healthcare and hospital stocks in India are experiencing unprecedented growth, surpassing mere survival to become key players in the stock market rally.