Executive / Sr. Executive / Asst. Manager - Regulatory Affairs

• Preparation of Dossier Document (CTD & ACTD) as per country specific Requirement.
• Review of QA & QC documents as per dossier requirement.
• Dossier preparation for ROW.
• To handle Query received from Various Country.
• Responsible for overall document to ensure that DRA & FDA records are evaluated & signed by an authorized person.
• Responsible to check & evaluate as per requirements & standards. Review and checking product specification.

Walk in on 5th February, 2022

Time:- 10:00 Am to 12:00 Pm

Venue:- Umedica Laboratories (R&D Centre)Pvt. Ltd, D-25/4, TTC Industrial area MIDC, Turbhe, Navi Mumbai – 400705.

Candidate who cannot appear walk in interview they can send their CV on given MailId.