The role is responsible for supporting regulatory affairs activities related to clinical trial supplies, regulatory documentation, product labelling, and coordination with internal teams and external stakeholders. The candidate will assist in reviewing regulatory requirements across different countries, maintaining documentation, and ensuring that clinical trial materials meet applicable regulatory requirements.

Qualifications
• Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, or a related field.
• Candidate must have 2–3 years of experience in Regulatory Affairs, preferably in the pharmaceutical, clinical research, or clinical supply chain industry.
• Knowledge of regulatory requirements for clinical trial supplies across different countries.
• Experience in preparing, reviewing, and maintaining regulatory documents, product labels, and packaging-related documentation.
• Familiarity with regulatory submissions, document control, and applicable guidelines.
• Good communication, coordination, and documentation skills.
• Proficiency in Microsoft Office and the ability to manage multiple tasks efficiently.
• Ability to work independently in a remote work setting.

📌 Regulatory Affairs Specialist (New Delhi)
🏢 Intrinseque Health
📍 New Delhi