
Regulatory affairs Officer

Regulatory affairs Officer1583
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About the Job
Skills
Preparation and compilation of DMF for US, EU, CEP, Canada, Japan, China, Brazil and other semi-regulated markets.
· Submission of technical data package and Applicant’s Part for semi-regulated markets
· Submission of response to deficiencies received from authorities and customers
· Periodic DMF updates (annual report for USDMFs and CEP renewal) and DMF amendments for post approval changes for US, EU, Canada, CEP and other markets
· Use of eCTD software’s and submission gateways like ESG & CESP
· Providing regulatory inputs in early development phase of APIs
· Review of change controls and technical data required for DMF submissions
· Collection and review of data (AMV, process Validation stability etc.) required for compilation DMF
· Preparation of LOA and commitment and data management
· Submission of change notification for customer.
· Tracking of changes in pharmacopoeia, regulatory guidance, current trends / regulatory expectations and identification of gaps
· Maintenance of database for regulatory submissions including customer notifications
· Well versed with current regulatory guidelines.
About the company
Industry
Pharmaceutical Manufactur...
Company Size
51-200 Employees
Headquarter
GURGAON
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