Responsibilities:

• Responsible for projects follow up with governmental department
• Assist in product registration and GMP licence submission

• Assist in the preparation of regulatory documents in English and/or Chinese
• Monitor project budget, obtain comparative quotations, liaise with suppliers/vendors and perform the procurement of equipment and laboratory supplies

• Handle ad hoc. tasks as assigned by management

Requirements:

• Bachelor's degree or above in Biotechnology, Biomedical Science, Biological Science or related Life Science disciplines
• At least 2 years working experience in biotechnology or pharmaceutical field

• Knowledge in GMP and related regulations would definitely be an advantage

• Proficient in spoken and written English and Chinese
• Self-motivated and able to work independently
• Proficiency in computer application such as Microsoft PowerPoint, Excel and Word