UMEDICA LABORATORIES PVT ltd
Regulatory Affairs Jobs
Position: Executive / Sr. Executive / Assistant Manager – RA
Qualification required: M Pharmacy (Pharmaceutics)
Required year’s of experience: 03 to 10
Required skills set:
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.
Date: 05th February 2022 (Saturday) Time: 10:00 AM to 01:00 PM
Venue: Umedica Laboratories (R&D) Center Pvt. Ltd., D-25/4, TTC Industrial area MIDC, Turbhe, Navi Mumbai 400705. > Contact Person: Mr. Pramod Rahangdale HR/Admin. L: (+91-22) 62811800.
Markets: ROW (LATAM, Russia, CIS, Philippines & Cambodia) and Regulated Market (Europe).
Work location: Nariman point (Mumbai) for ROW & Turbhe (Navi Mumbai) for Regulated market.
Pharma formulation experience background is must required, good in communication skills and expected Industrial technical knowledge.
Interested candidates are requested to bring
Current CTC Proof / Salary Slip.
(All documents are requiring original & photo copy).
Candidates already attended Interview with Umedica within last three months are not to be considered as eligible for now schedule.
Those who are not able to attend walk in interview on scheduled date and time, may please send resume On email@example.com / firstname.lastname@example.org (Wearing a facemask is mandatory)
To apply for this job email your details to email@example.com