Key Responsibilities:

• Independently develop manufacturing processes for active pharmaceutical ingredients (APIs); proficiently optimize chemical reactions and resolve technical challenges encountered during experiments.

• Prepare samples from gram to hundred‑gram scale to ensure timely material supply for early non‑clinical studies.

• Comply with laboratory daily management regulations and maintain timely and accurate experimental records.

• Collaborate closely with key raw material suppliers to ensure uninterrupted material availability.

• Execute technology transfer of API processes; guide CDMOs in pilot‑scale production, as well as toxicology batch and GMP batch manufacturing.

• Systematically organize process development and production data; draft R&D reports and patent documents as required.

Qualifications:

• Master’s degree or above in Organic Chemistry, Medicinal Chemistry, or a closely related field.

• Minimum 3 years of hands‑on experience in API process development and production.

• Solid knowledge of organic chemistry and strong process development capabilities, with proven ability to solve diverse problems arising during process development.