Your new role

• Drive drug & medical device registrations and variations in accordance with relevant regulations and develop strategies to obtain the product approval within target timeframe.

• Maintain products’ licenses in responsible countries

• Keep abreast of regulatory procedures and product changes to ensure registration dossiers are maintained in compliance with local and corporate instructions.

• Effectively communicate and collaborate with local RAs and HQ RA team in France and US in order to develop Regulatory Strategies

• Provide local regulation intelligence to internal stakeholders

• Ensure company’s products comply with the regulations

• Plan and coordinate packaging changes with related departments
• Ensure validation of promotional materials in compliance with local regulations and corporate policy.

What you'll need to succeed

• Bachelor’s degree in health-related science, life science; Pharmacist or related academic background is preferred

• 3–4 years of relevant experience in pharmaceutical registration and experience in medical device registration in ASEAN countries and/or Hong Kong is preferred

• Excellent verbal and written communication skills in English and Cantonese
• Proficient in MS Office, including Word, Excel and PowerPoint
• Previous experience in a multinational environment
• Effective communication and interpersonal skills

What you need to do now

If you're interested in this role, please send your updated CV to rooney.wu@hays.com.hk