Designation: Executive – RA (2 Employees)Qualification: B. Pharm / M. Pharm RAExperience: 2 to 3 YearsJob
Description: · Preparation and review the dossier of as per current prescribed guidelines of the respective
regulatory authority.· Well versed with the guidelines of ICH and other regulatory.· Preparation of documents for license application.· Preparation of documents for COPP, FSC and other legal documents
including product permission· Preparation of registration documents as per ACTD , CTD , country
format / Review / Preparation & Compilation· Preparation of text matter and checking of artworks.· Should coordinate with factory for samples, working standards, document
data, license related documents.· Should have knowledge with regard to checking of samples.· Courier of documents and samples to respective customer.· Maintaining status and record of dossiers, samples legal documents.· Reply of queries.· Co - ordinate with regard to legalization of documents.· Maintaining record of registration status and re - registration. · Dossier Submission and Query Response

📌 Regulatory Affairs Executive Vadodara
🏢 Recognized
📍 Vadodara