FEATURED JOBExecutive
Cadila Pharmaceuticals Ltd
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Applied
Posted: 17 Dec 25
Job Description
· Preparation and submission of new DMF as well as annual updates to global markets including US , EU, Japan, China and Korea
· Preparation and submission of CEP applications and responses to EDQM via CESP.
· Preparation and submission of amendments to DMF for various regulatory authorities including less regulated market authorities.
· Preparation of responses on the queries raised by customers and regulatory authorities on drug master files.
· Collection and compilation of documents to prepare Regulatory submissions and customers.
· Preparation of applicant’s part for regulated markets and less regulated markets.
· Preparation and submission of LOA’s, CEP LOA’s and declarations for various customers and authorities.
· Preparation and submission of SPLs for US FDA authority.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2809498
Job Category Sales and Marketing
Locality Address
State
Country India
About Company
Cadila Pharmaceuticals Ltd
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