1. Process scale-up and technology transfer for biologics products (primarily mammalian cell- culture based products) from R&D to manufacturing
2. Manufacturing process monitoring and continuous process verification
3. Identification of manufacturing process improvement opportunities and implementation of process improvements
4. Lead all manufacturing process related technical investigations
5. Lead cross-functional teams between R&D, Manufacturing, Quality and Regulatory for technology transfer projects
6. Provide support for regulatory dossier preparations, regulatory agency audits of the GMP facility, etc.
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