Sun Pharma Walk-in Interview for Regulatory Affairs | Baroda - PHARMA STUFF

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Nov 21, 2024

Sun Pharma Walk-in Interview for Regulatory Affairs | Baroda

sun-pharmaceutical-industries-recruitment-notification 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
[caption id="attachment_56281" align="aligncenter" width="930"]sun-pharmaceutical-industries-recruitment-notification Sun Pharma Walk-in Interview for Regulatory Affairs: Exciting Career Opportunities[/caption]

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.
https://pharmastuff.org.in/job/sun-pharma-walk-in-regulatory-affairs