About Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anaesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

What You’ll Be Doing

It’s impossible to list everything you’ll do here because every day is different. But a few things are clear, you’ll:

• Responsible for managing pharmaceutical drug, biological products and medical device registrations in Hong Kong and Macau

• Lead a team to perform all kind of RA related matters

• Ensure products are in compliance with regulations and systems are in compliance with Standard Operating Procedures and local Hong Kong regulations.

• Planning of regulatory strategies to support business needs

• Provide professional advice to organization on Pharmaceutical Ordinances and Legislations

• Support Business Units in strategy planning and government tenders

Do you have what takes to build a career here?

• Degree holder in Pharmacy and Master degree holder in related fields.

• At least 8 years working experience with Regulatory affairs in pharmaceutical industry and at least 2 years in supervisor level

• Good command of written and oral English and Mandarin

• Possess very strong business acumen;

• Be confident & willing to take challenges, smart working, passion to work, and able to work under pressure with multi-task;