<p>1. Responsible for reviewing and determining the raw material development plan for the R&D project.</p>
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<p>3. Continuously follow up on and understand the processes and regulations related to generic drug development and product application, and participate in the writing and modification of application materials.</p>
<p>4. Familiar and master the laboratory safety regulations, correctly operate various instruments and equipment.</p>
<p>5. Actively cooperate with the department and other departments in communication and cooperation, and complete project application-related work. </p>
<p>6. Collaborate with project management related data statistics and other related work, complete other tasks assigned by the leader.</p>
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<ol>
<li>Be responsible for the review and determination of the raw material development plan for the R&D project.</li>
<li>Be responsible for the synthesis required for API (Active Pharmaceutical Ingredient) registration, process optimization and purification, as well as pilot-scale-up production. And be responsible for the specific implementation of the chemical API of the R&D project at the base.</li>
<li>Continuously follow up on the processes and regulations related to generic drug R&D and product registration, and participate in the preparation and modification of registration documents.</li>
<li>Be familiar with and master the laboratory safety regulations, and correctly operate various instruments and equipment.</li>
<li>Actively cooperate with the communication and cooperation between the department and other departments, and complete the work related to project registration.</li>
<li>Cooperate with the relevant data statistics of project management and other related work, and complete other tasks assigned by the leader.</li>
<li>Relevant experience in generic drug projects (which can also be project management) is required, and the ability to comprehensively arrange generic drug API projects is needed.</li>
</ol>
<p>BASE: Guangzhou Huangpu District</p>