Sun Pharma Walk-in Interview for Regulatory Affairs | Baroda

Sun Pharmaceutical Industries Ltd., a global leader in the pharmaceutical industry, is conducting a walk-in interview for Regulatory Affairs roles across multiple levels.

Walk-in Interview Details

• Date: Sunday, 24th November 2024
• Venue:
  Sun Pharmaceutical Industries Ltd.
  Sun Pharma Road, Tandalja, Baroda – 390016

Note: Candidates unable to attend the interview can share their resumes at Hr.Tandalja@sunpharma.com.

Available Positions and Requirements

Regulatory Affairs – US and Europe Market

• Designation: Executive/Senior Executive
• Qualification: M. Pharm
• Experience: 1-8 years
• Location: Baroda
• Designation: Manager
• Qualification: M. Pharm
• Experience: 9-13 years
• Location: Baroda

Plant Regulatory Affairs

• Designation: Senior Executive/Manager
• Qualification: M. Pharm/B. Pharm
• Experience: 6-10 years
• Location: Halol

Key Responsibilities

1. Dossier Compilation and Review:
   • Compile and review dossiers for US, EU, AU, Canada, and IL markets.
   • Oversee query responses prepared by regulatory associates.
2. Team Management:
   • Allocate projects to associates and manage regulatory submission activities.
   • Monitor the lifecycle management for assigned markets.
3. Regulatory Submissions:
   • Ensure timely dossier submissions and query responses.
   • Coordinate with cross-functional teams (CRA, ADD, MSTG, PMO, etc.) for regulatory compliance.
4. Stakeholder Coordination:
   • Collaborate with plant teams for data compilation and sample requirements.
   • Participate in action plan discussions and submission timelines for regulatory queries.
5. Lifecycle Management:
   • Oversee document compilation for new product filings, renewals, and re-registrations.
   • Monitor circulation of regulatory approvals and commitment details to plant teams.