Roles and Responsibilities
Responsible for preparation & compilation of the dossiers in CTD/eCTD/ACTD and other formats as required for submission to different regulatory authorities.
Review the documents i.e. Specifications, Batch Records, STP, Stability Protocol, Dissolution protocols & DMF documents etc.
Preparation of pharmaceutical/quality part (all forms) of registration dossiers & variations/amendments/annual reports as applicable documents in CTD and eCTD format.
Preparation of query response for submitted applications received from various regulatory authorities.
Responsible for review of change controls and checking for regulatory compliance for all documents.
Exposure of Dossier compilation for ACTD & CTD is mandatory.




Coordination with the external stakeholders for the preparation of the regulatory documents.
To be responsible for the Life cycle management of assigned products.
Should have experience for Life cycle management and license Maintenance.
Should have valuable knowledge for recent guidelines, websites and trends of Europe, Africa, Mexico, LATAM region, Chile, Costa-Rica, Peru, Panama, Asian, CIS market.Role & responsibilities

Desired Candidate Profile:
Candidate must have valuable knowledge of working in Europe, Africa, Mexico, LATAM region, Chile, Costa-Rica, Peru, Panama, Asian, CIS market.

📌 Regulatory Affairs Executive Ahmedabad
🏢 Medwise Overseas
📍 Ahmedabad