Designation and Department: Officer – Regulatory Affairs
Qualification : B.Pharma
Experience- 2-3 Yrs
Job Description
1. Preparing, reviewing and submitting product dossiers as per CTD ACTD and ROW market requirements
2. Preparing, reviewing and submitting renewal documents/renewal dossiers/ variations/responding to queries raised by Ministry of Health, International agencies as well as the various customers.
3. Involved in co-ordination with Plant, R&D and QA-QC Department for preparation and receiving & reviewing of technical Documents such as DMF, Stability data, etc. and sample arrangement for dossier submission
4. Approval of artworks.
5. Tender submissions.
Interested Candidate Share your cv on latesh.nemade@skant.com or megha@skant.com
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