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R & D CMC Regulatory Affairs Chemical Products Scientist / Sr. Scientist
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- R&D CMC Regulatory Affairs Chemical Products Scientist/Sr. Scientist
- As a staff member of CMC Regulatory Affairs Department of Japan Development Division, a person in charge who is willing to contribute in CMC Regulatory Affairs (RA) tasks from initial stage of new drug development to NDA filing and the approval, addition of dosage form, and change controls.
- We can offer a range of opportunities to experience product development with a cutting-edge CMC technology and/or to be in front line of discussion on regulatory CMC topics which are focused on in the pharmaceutical industry.
- Identify product issues and assess risks from the CMC viewpoint, and plan countermeasures.
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