Job Duties:

• Responsible for the development of analytical methods for pharmaceutical products, draw up the working plans and schedules for quality research.
• Responsible for drafting specification, validation documentation of analytical methods, and submission documentation related to quality research. 
• Prepare and review of CTD submission documents, chromatograms, raw data records, etc.
• Assist in performing instrument calibration and maintenance
• Perform day to day general laboratory activities
• Prepare protocols & reports or any related document
• Manage projects effectively according to the project timelines

Job Requirements:

• Master or MPhil or PhD in Pharmaceutical Science, Analytical Chemistry or related areas
• At least five years’ experiences of analytical methods development and quality research of pharmaceutical products
• Proficient in analytical instruments such as HPLC, GC, etc.
• Possess laboratory management experience and have a strong sense of R&D quality system compliance
• Familiar with relevant pharmaceutical guidelines and regulations for NMPA CDE and ICH. Ability to develop research plans and schedules effectively, break down and arrange work according to the research plan, and implement concretely
• Have an overall experience in development of oral solid pharmaceutical product and related project management skill, and be able to manage multiple projects simultaneously
• Strong sense of responsibility, excellent communication and team management skills
• Good ability in data interpretation, trouble shooting and problem solving

Work location: Yuen Long 

Shuttle bus pick up point: Quarry Bay / Lam Tin / Kowloon Tong / University Station / Long Ping Station

We are an equal opportunity employer and all information collected will be used for recruitment purpose only.