Job Responsibilities
- Participate in quality assurance monitoring program, validation and qualification work of facilities, equipment, in order to ensure compliance with GMP standards.
- Provide GMP training and follow the training program.
- Prepare for quality GMP documents.
- Involve in document control by executing the issuance, distribution, withdrawal of document and maintain the document index database correspondingly.
- Conduct data entry and data analysis for reports / reviews.
- Assist in the procedure of releasing finished products.
- Perform other duties assigned by the supervisor(s).
Job Requirements
- Higher Diploma or above in Science subjects, preferably in Pharmaceutical Science, Chinese Medicine, Biotechnology, Biochemistry.
- At least 1 year of relevant experience in the pharmaceutical industry.
- Positive mindset, able to be a good team player.
- Good command of English and Chinese, both spoken and written.