Job Description

Division
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IPD Department
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IPD Employment Type
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Permanent Job Purpose
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Submit product documents to regulatory authorities in accordance with country specific regulatory requirements to ensure approvals and market launch in stipulated time and handle post-approval changes, maintenance, and updation of documents during the products life-cycle

Accountabilities
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I. Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by reviewing, collating, and compiling documents in order to ensure approvals for launch in stipulated time

II. Submit post approval variations for changes that improves productivity, cost-effectiveness, quality of the product by reviewing, collating, compiling the variation application to meet the delivery within timelines and maintain Product Marketing Authorization, Renewals/Sunset clause to ensure continuous validity of marketing authorisations.

III. Maintain, and update product dossier as required to meet changes in Ciplas internal systems, changes in regulatory guidelines, and to meet the need of regulatory requirements

IV. Update the database (PRC/SAP-RA/ table) associated with product dossier approvals by including registration details in database.

V. Provide Regulatory support throughout the life cycle of the product for smooth functioning

VI. Provide the informatuitability and availability of dossier for out-licensing and in-licensing

VII. Check with regulatory authorities (EU, NZ & TGA) for submission activity and approval status for submission done

Education Qualification
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B.Pharmacy, M. Pharm, Bsc or MSc

Relevant Work Experience
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Minimum 5 years' experience in regulatory activity in pharma industry preferably worked for same region/authority

Competencies/Skills
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Collaborate to Succeed
Innovate to Excel
Perform with Accountability
Lead with Empathy
Act with Agility
Strong Domain Knowledge
People Management Job Location
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Vikhroli

Shift Hours
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