Nanz Pharma Job Opening For Regulatory Affairs Department
Urgent Opening - Regulatory Affairs- Manager
JD/ Exposure -
NDCT 2019, New Cosmetic rules 2020 and MDR 2017 Preparation and filing of CTD Dossier in various ROW countries
Filing New Drug/SND Applications in CDSCO & presenting Clinical protocol in SEC.
Test & Manufacturing licence for all Drugs & Rapid Diagnostic Kits & optimization
• Import/mfg. Licence Applications for IVD & MD as per Medical Devices Rules 2017 on Sugam Portal.
. preparation of Device Master File, Device History Files, EP Checklists & SMF as per Medical Devices Rules 2017 with current regulatory requirements.
Expertise in overseeing documentation to ensure compliance with domestic and international regulations and standards.
Experience.- 10-12 Yrs
Edu. Qualificatios- M. Pharma/ DRA
Salary- Best in the industry
Interested candidates send cv on below mail id
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