[Nh-949] - Regulatory Affairs Technician

Specific Responsibilities: Collection of information necessary for the preparation of registration documents ASMF/DMF/CEP.Monitoring procedures pre and post authorization of the products of the company.Answers deficiencies letters sent by the health authorities.Technical support to the sales department with the technical requirements of the customers.Direct development of product registration submission, progress reports, supplements, and amendments.Advises development and/or production and/or quality teams on manufacturing changes, appropriate regulations, and interpretations.Management of the customer enquiries through CRM according to the internal policy.Fluent and timely communication with internal and external partners (QA, commercial, etc).
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