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 sub-teams as a representative of the RA for providing regulatory support for the ongoing projects.

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