An Associate Regulatory Affairs Manager position from a global MNC pharmaceutical company.

Your new company
Our client is a global speciality pharmaceutical company that aiming to manufacture high quality and affordable products to improve health of patients in the world.

Your new role
Based in Hong Kong and reporting to the Regulatory Affairs Manager, act as a regulatory expert that responsible for handling end- to-end regulatory and Pharmacovigilance activities of the assigned portfolio in Hong Kong.

• Coordinate complete registration activities of company products (pre- and post-approval, withdrawal)
• Maintain regulatory records and database with updated product registration status and registered product information
• Establish close interaction with key government authorities to deliver submission and advocate significant business goals
• Work with internal regulatory team to ensure prompt product registration
• Assist in ad-hoc regulatory affairs and Pharmacovigilance project assigned by line manager

What you'll need to succeed

• Bachelor's degree or above in life science related disciplines, major in pharmacy will be an advantage
• At least 3 or more years in an international or local pharmaceutical company
• Good knowledge on application laws & regulations, regulatory practices and industry codes in Asia region
• Attention to details and well organised
• Communication skills to adopt changes in regulatory requirements
• Fluent in English and Cantonese

What you need to do now
If you are interested in the above opportunity, please forward your latest resume to [email protected] or contact Kristi at +852 2230 7904 for more information.

If this role isn't quite right for you but you are looking to explore new opportunities in the life science sector, please contact Kristi Pang for a confidential discussion about your options.

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