Senior Medical Affairs and Regulatory Affairs Specialist

Senior Medical Affairs and Regulatory Affairs position for a well-known MNC pharmaceutical company
Your new company
You will be joining a reputable international pharmaceutical organisation focused on advancing treatments in Hong Kong. The company is committed to scientific excellence, patient safety, and strong collaboration across commercial, medical, and regulatory functions.

Your new role
You will be responsible for driving all medical affairs activities and ensuring scientific credibility across the market. You will work independently to make critical decisions that support business objectives while upholding the highest compliance standards.

Medical Affairs
  • Conduct field visits with Marketing and Sales teams while engaging and addressing enquiries from healthcare professionals
  • Deliver scientific presentations and communicate unique product advantages to HCPs
  • Manage and resolve product‑related queries from authorities, HCPs, and the public
  • Play an integral role in pre‑launch planning and launch execution for new products
Training & Scientific Development
  • Lead product knowledge training and updates for staff
  • Provide pipeline and strategic product briefings
  • Oversee annual training programmes and SOP refreshers
Regulatory Affairs
  • Oversee new product registrations and variations
  • Monitor product patent statuses and coordinate legal follow‑up when needed
Compliance
  • Ensure all interactions with HCPs and vendors meet internal and external compliance standards
  • Review and approve promotional, non‑promotional, educational, and HCP presentation materials
What you'll need to succeed
  • Master’s degree in Pharmaceutical Science, Medical Sciences, or a related healthcare discipline (Bachelor’s degree with strong experience will also be considered).
  • Experience in regulatory affairs, clinical trials, pharmacovigilance, and compliance is highly advantageous.
  • Strong leadership capabilities with the ability to coach and influence cross‑functional teams.
  • High level of independence, responsibility, and decision-making maturity.
  • Excellent project management, time management, and problem‑solving skills.
  • Strong communication, interpersonal skills, and the ability to work under pressure.
  • Fluency in Cantonese, with excellent verbal and written English and Chinese.
What you'll get in return
  • A highly independent role with significant strategic influence on business growth.
  • Close collaboration with regional and cross‑functional teams, offering strong career development potential.
  • A dynamic, purpose‑driven environment focused on science, compliance, and patient safety.
  • Competitive compensation and benefits aligned with your experience and expertise.
What you need to do now
If you are interested in the above opportunity, please forward your latest resume to Kristi.pang@hays.com.hk or contact Kristi Pang 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 for a confidential discussion about your options.
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
HongKong
Specialism
Life Sciences
Ref:
1284248

Talk to a consultant

Talk to Kristi Pang, the specialist consultant managing this position, located in Hong Kong
6604-06,66/F, ICC, 1 Austin Road West, West Kowloon

Telephone: +85222307904

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