FEATURED JOBExecutive
Cadila Pharmaceuticals Ltd
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Posted: 24 Jul 26
Job Description
JOB RESPONSIBILITIES
• Compilation, review and submission of registration dossiers in the regions of South East Asia.
• Handling of regulatory queries/deficiencies across all the South East Asia countries.
• Submission of Supplements/Variations across all the South East Asia countries.
• Review of functional documents such as Specifications/Test Procedures/Product Development Reports/Stability Protocols etc. and Review and approval of Change Controls & Deviations.
• Ensure availability of current guidelines for South East Asia.
• Establish co-ordination with other departments like QA/QC, R&D, Marketing and Purchase for
ensuring the filings and query response within period.
• Submission of various original documents for notarization, chamberization and legalization, which forms an important part of dossier.
• Arrangement of Samples, Packing Material, Impurities, Reference Standards as per MOH
requirement.
• Preparation of COPP’s (Certificate of Pharmaceutical Product) and FSC submit to Local FDA
approvals.
• Any other assignments as specified by the reporting authority from time to time.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2929494
Job Category Sales and Marketing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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