Base pyy: not specified; location dependent ranges...
Not specified (assumed to be hybrid based on regulatory roles)
5 years pharmaceutical regulatory experience
Drug product registration submission management
Post-market compliance and change control
Abbott is seeking an Associate Regulatory Affairs Manager in Beijing, China, responsible for ensuring timely drug product registration and compliance with post-market regulations. The ideal candidate will have a strong background in pharmaceutical regulatory affairs, with a focus on collaboration and communication across various functions
Job Summary
The primary goal is to secure drug product registration submissions and approvals on time to ensure business continuity.
The role requires managing post-market regulatory compliance including formulation, labels, and promotional materials while engaging with health authorities.
Candidates must possess strong bilingual communication skills in English and Chinese to effectively negotiate and collaborate across diverse disciplines.
Matching Summary
Match Score: 85
Abbott is seeking an Associate Regulatory Affairs Manager in Beijing, China, responsible for ensuring timely drug product registration and compliance with post-market regulations. The ideal candidate will have a strong background in pharmaceutical regulatory affairs, with a focus on collaboration and communication across various functions.
Salary
Base pay: Not specified; Location dependent ranges may vary; Benefits: Not specified
Skills & Requirements
Must-have
5 years pharmaceutical regulatory experience
Drug product registration submission management
Post-market compliance and change control
Health authority interaction and negotiation
Bilingual English and Chinese communication
Nice-to-have
Advanced degree in life sciences
Experience with internal legislation databases
Strong analytical and project planning skills
Ability to lead cross-functional teams
Proficiency with electronic regulatory systems
Key Requirements
Bachelor's degree in pharmacy, chemistry, biology, or related life sciences
Minimum of 5 years experience in pharmaceutical regulatory affairs