Sun Pharmaceutical Industries Limited
WALK-IN DRIVE @ Baroda
Department:
Regulatory Affairs - US, Canada, EU, Australia and Israel, Regulatory - EM
Qualification: M.Pharm
Experience: 2-7 years
Brief 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 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 approval
•New submissions
•Approvals
•Lifecycle management for drug formulations:
•Regulatory compliance
Date of Interview: Sunday, 5th May 2024
Time: 9.30 am - 1.00 pm
Venue:
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
Disclaimer: Sun Pharma does not seek payment of any kind from any prospective candidate for employment or authorize any agency or any individual to collect or charge fees for recruitment. Please be cautious while dealing with any recruitment agency or anyone asking you to pay money representing Sun Pharma. Merely participating in any recruitment drive does not ensure job entitlement at Sun Pharma
Email your resume at: Hr.Tandalja@Sunpharma.com
