Johnson & Johnson Careers

Regulatory Affairs Assistant Manager

Beijing, Beijing
Regulatory Affairs


Job Description

Requisition ID: 1805655372W

• Provide innovative regulatory strategies/ direction to the business for relevant con-sumer drug products.
• Connect with global and regional colleagues to develop regulatory strategy and pathway to speed up products to market in China, and support in market products to ensure compliance.
• Work with global/ regional/ local colleagues to identify core processes and support required to ensure projects can be aggressively implemented in China with greatest commercial impact.
• Lead relevant RA subgroup and take care of people development for regulatory team.
• Involve in external engagement, sitting as key company representative in several in-dustry associations to deliver JnJ voice and drive china regulatory reform.
• Organize key external projects with authorities and associations to build JnJ high pro-fessional image and credibility on technical/regulatory issues.

Qualifications
  • Bachelor or above, Chemical/ Pharmaceutical/biological background is preferred.
  • At least 5 years working experience in pharmaceutical product registration especially in new drug/creative drug registration, familiar with CFDA registration requirements.
  • MNCs and OTC registration experience is preferred.
  • Fluent IT skills on Microsoft office, Outlook and internet operation.
  • Sufficient in English reading and writing.

Primary Location
China-Beijing-Beijing
Organization
Shanghai Johnson & Johnson Pharmaceuticals, Ltd. (7048)
Job Function
Regulatory Affairs
Requisition ID
1805655372W