Responsibilities

. Responsible for the whole-process management of production materials, consumables, semi-finished products and finished products in strict accordance with GMP requirements

. Mastery of the principles of DP equipment, familiarity with the production process, you may be able to operate equipment independently and perform basic maintenance of related equipment

. In accordance with GMP requirements, draft and revise related operating procedures, batch production records and related files

. Strictly adhere to change control and deviation investigation process, organize the drafts and implementation of changes, conduct deviation investigations, and establish corrective and preventive actions

. Analyze and solve problems arising in the manufacturing process independently and understand how to contribute to solving problems and optimizing the process through literature review

. Continuously optimize production processes and workflows to ensure production quality and improve production efficiency

. Familiar with project production and transfer processes, capable of conducting gap analysis and project transfer

. As a project lead, communicate internally and externally with other departments and clients to ensure the effective implementation of the project and solve the problems arising in the project

. Participate in designing and recommending new plants

. Participate in audits related to DP manufacturing

. Adherence to company compliance requirements

Requirements

. Bachelor's Degree with a major in any of the relevant disciplines: Pharmaceutical Manufacturing, Pharmaceutical Engineering, Pharmacy, Bioengineering, Biotechnology, Chemical Engineering, Microbiology, etc.

. Knowledge of GMP is preferred, and expertise in aseptic production is an advantage.

. Solid foundational knowledge in pharmacy and biotechnology, with proficiency in Microsoft Office.

. Good English language skills, literature review skills, and a proactive approach to problem-solving in the workplace.

. Strong hands-on operational ability, with careful and conscientious equipment operation and timely record-keeping.

. Good communication and presentation skills.

. Strong team collaboration, efficient execution, and a great sense of ownership.

Career Development

. Comprehensive in-house training program (E-learning / OJT / Mentorship)

. Dual career development tracks - Professional & Managerial Tracks

. Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment

. Cross cultural learning

. GMP greenfield start-up experience

Associate Manufacturing Engineer - Drug Product