Regulatory Executive (Med Tech)

0 years

0 Lacs

Posted:1 month ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Responsibilities: Approval of QMS Documentation for Medical Devices. Guidance to draft documents for the Form MD - 12, MD - 7 and MD - 3 for CDSCO submission. Guidance to draft products instruction for use. Guidance to draft Product Labelling. Conducting Training for applicable standards. Review of Risk Management file. Review and finalization of product dossier for USFDA submission Conducting Management Review Meeting. Show more Show less

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Topia Life Sciences logo
Topia Life Sciences

Biotechnology

San Diego

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