Job Description
Design and optimize the formulation of solid and liquid pharmaceutical products.
Conduct stability studies, pre-formulation, and compatibility tests.
Prepare technical documents for product registration and transfer of the formula to production.
Cooperate with production, quality control, quality assurance, and RA units.
Work with production equipment such as tablet press, coater, blender, etc.
Review and apply international pharmacopoeia standards (USP, BP, EP).
Comply with GMP requirements and accurately document processes.
Requirements:
At least two years of work experience in a related field.
Familiarity with physical and chemical tests of the final product.
Familiarity with pharmaceutical documentation and documentation registration.
