Key Roles and Responsibilities

• To assist in developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) and other production documents
• To ensure and maintain the adequate and accurate records for controlling and monitoring conformity to specified GMP and statutory requirements
• To assist monitor the production process according to the production plan
• To participate on performing qualification and validation activities and prepare relevant documents
• To perform the daily operation and ad-hoc functions of Production Department

Qualifications and Experience

• Higher Diploma holder or above in Science/Engineering disciplines.
• Fresh graduates will also be considered as Assistant Production Officer
• Relevant experience in GMP pharmaceutical manufacturing is preferred
• Familiar with MS office and Chinese word processing
• Hardworking, initiative, self-motivated and fast learner
• Able to work under pressure and willing to work overtime
• Good interpersonal skill and communication skill

How to Apply

You are invited to send in your application and CV stating the position (with reference number) you are applying for together with your current and expected salary, either by clicking "Apply Now" on or before 30 April 2018.

Medipharma Limited is an equal opportunities employer. The information provided will be treated in strict confidence and used only for consideration of application for relevant/similar post(s).  All personal data of unsuccessful applicants will be destroyed within 6 months.