Job Description 1. Preparation of applications and documents for registration of Recombinant Products in Regulated and Semi-Regulated Countries. 2. Preparation of documents required for RA Compliance CMC guidelines / Dossier preparation guidelines and Assisting in CMC Compliance activities. 3. Coordination with customers, and regulatory bodies of various countries. 4. Participates in the multi-disciplinary product development…Apply Here >>
Build your career in Clinical Research
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