Job Title:
Executive - Regulatory and Business Continuity
Business Unit:
R&D1; Regulatory Affairs
Job Grade
G12A
Location:
Baroda
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
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.”
Key Responsibilities:
- Compilation, review of dossier for US, EU, AU, Canada & IL market for both solid oral and non-oral dosage form
- Review of query response prepared and compiled by regulatory associates
- Manage all the activities pertaining to dossier submission for aforesaid markets.
- Meet the dossier submission and query response timeline as per given target
- Review of all the documents received from stake holder for dossier compilation, Query response and Life cycle management
- Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
- Lifecycle management for US, EU, Canada & IL market
- Single point contacts for all the regulatory submission activities for IL and Palestine markets
Travel Estimate
NA
Job Requirements
Educational Qualification
M.Pharm
Experience
- Tenure_: 2 - 4 yrs.
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 qualified 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_