Senior Executive- India Regulatory Affairs

About the role

Manager II – India Regulatory and business Conitnuity Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

What you'll do

• Evaluate regulatory strategy for products to be registered in India
• Co-ordinate with Cross Functional Team for getting various documents required for filing the product in India
• Responsible for reviewing CMC documents to be submitted in dossier as per regulatory guidelines
• Review specification for bulk drug and formulations as per regulatory expectation
• Responsible for reviewing clinical trial and bioequivalence study documents to be submitted in regulatory applications

What you need

• Regulatory affairs
• Any graduate