R&D- GRA- Associate Regulatory Affairs Manager - BJ

Sanofi
北京市
全职
3周前

Resiponsible for new product registration projects and LCM of marketed products in China:

 

To coordinate with other departments such as Medical and Marketing Department during the registration process to share necessary information for registration.
 

To maintain efficient and durable relationships with government authorities such as NMPA, NIFDC, CDE, CCFIDE to ensure a smooth registration process.
 

Eusure compliance during the all registration activities.

 

The jobholder faces an evolving legislation and changing regulations on vaccine administration. Therefore, he/she needs to keep updating his/her knowledge on the latest regulations.

 

He/she should be able to considerate problem and control project process independently and systematically. Provide decisional suggestions and has strong executive force.

 

What you should have?

If you are a person demonstrate respect, teamwork, courage and intergrity with special focus on below competency:.

Team player with good communication, negotiation and influencial skills

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

申请
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