Pharma R&D Scientist — Formulation, Trials & Registration

Jacobson Medical (HK) Ltd; Sha Tin; On-site; HKD 300,000 - 520,000; Full time

Job summary

Jacobson Medical (HK) Ltd in Hong Kong seeks a qualified pharmaceutical scientist to lead new product literature research and development. You will prepare research proposals and drive project studies across formulation, process development, quality control, and stability, supporting registration and clinical trials.

The role requires strong analytical skills, regulatory familiarity, and fluent English/Cantonese/ Mandarin, with immediate availability preferred.

Qualifications

• Bachelor's degree or above in pharmacy, chemical analysis and related subjects.
• 3 years related experiences.
• Experience about pharmaceutical method development and validation.
• China registration experience is highly preferred.
• Familiar with laboratory analytical instruments, e.g. HPLC, GC, HPLC-MS etc.
• Knowledge of registration regulations by SFDA, ICH, FDA.
• Good command of both spoken and written English, Cantonese and Mandarin.
• Immediate available is highly preferred.

Responsibilities

• Responsible for new product literature research and new product development.
• Prepare new product research proposal.
• Complete project research, including but not limited to preparation of trial proposal, pharmaceutical experimental research e.g. formulation, process, quality control, and stability etc.
• Prepare samples for registration and clinical trials.
• Responsible for trial production and technology transfer of the assigned project and assist market launch.
• Provide technical support to relevant departments and Business Units.
• Manage corresponding work and assist with the development and perfection of department system.
• Ad hoc projects as assigned.

Education

Bachelor's degree or above in pharmacy, chemical analysis

Tools

HPLC

GC

HPLC-MS

Job description

Jacobson Medical (HK) Ltd in Hong Kong seeks a qualified pharmaceutical scientist to lead new product literature research and development. You will prepare research proposals and drive project studies across formulation, process development, quality control, and stability, supporting registration and clinical trials.

The role requires strong analytical skills, regulatory familiarity, and fluent English/Cantonese/ Mandarin, with immediate availability preferred.