Executive/Sr.Executive

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.”

Key Responsibilities

Review all data and documents related to product registrations for various health authorities.

Compile registration dossiers for submission to various health authorities like – US-FDA, Health Canada, Europe, Australia/New Zealand, Japan and Israel.

Prepare responses to deficiency letters received from various agencies.

Maintain life-cycle / post approval changes for drug product registration dossiers.

Provide regulatory support to cross functional departments.

Prepare and submit scientific advice to various health authorities.

eCTD compilation, verification and submission through electronic gateway

Review, preparation and submission of annual reports to US FDA

Review, preparation and submission of post approval supplements to US FDA

Job Requirements

Educational Qualification –

B. Pharma / M. Pharma

Experience –

Tenure: 4-6 Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!