Job Information
BD (Becton, Dickinson and Company) RA_法规事务专员_北京 in Beijing, China
Job Description Summary
Responsible for Imported BDI_PI Products Regulatory Affairs
Job Description
KEY RESPONSIBILITIES （主要职责）
Maintain current NMPA approved certificates, including extension registration, change registration and support BU&RC to resolve post-marketing issues.
Make charge of new products launch in China, including make strategy, control registration timeline, type test, prepare registration documents, following evaluation and get approval.
Host regular meeting with WW to get requested documents and update registration status.
Follow NMPA regulations and analysis impacts to BD or responsible products. Other affairs within the team.
SKILLS AND ABILITIES （技能）
Medical/Pharmacy background, relevant experience on regulatory affairs
Bachelor degree or above
At least 2 years of regulatory affairs experience
Proficient in spoken and written English and Chinese
Ability to work independently and experience in a team on multiple projects Excellent interpersonal and communication skills
DESIRABLE （优先条件）
Medical device company working experience
Overseas education background
Required Skills
Optional Skills
.
Primary Work Location
CHN Beijing
Additional Locations
Work Shift
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.