Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications for the world. We are hereby inviting candidates who are interested to join India’s No.l company in Pharmaceutical Sector.
WALK-IN DRIVE @ Baroda
Regulatory Affairs – US, Canada, EU,Australia and Israel
Qualification : M.Pharm
Experience : 2 - 7 years
Job Description
Review all data and documents related to product registrations for various health authorities.
• Compile registration dossiers for submission to various health authorities like – USA, Canada, Europe, Australia 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
Regulatory - EM
Qualification : M.Pharm
Experience : 3-7 years
Job Description
Regulatory submission of new products, variations, renewals, response to queries, Life cycle management for South Africa and Singapore (APAC) markets through preparation of quality dossiers enabling timely approvals.
1. New submissions
2. Approvals
3. Lifecycle management for drug formulations
4. Regulatory compliance
Date of Interview : Sunday, 5th May 2024
Time : 9.30 am – 1.00 pm
Venue of Interview : Sun Pharmaceutical Industries Ltd –Sun Pharma Road, Tandalja –Baroda -390016
Note : Candidates are requested to walk in with updated resume, last degree, PAN card, Aadhar card and current CTC proof at the venue
Email your resume at: Hr.Tandalja@Sunpharma.com
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