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

SEND YOUR RESUME BELOW

Nov 21, 2024

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

 

Regular Pharma job updates on your mobile join below groups


What's app group                   click here


Instagram                                 Click here

 

Facebook page                         Click here

 

Linkdin                                       Click here


Facebook group                       Click here


Telegram                                   Click here


YouTube                                   Click here