R&D
R&D-GRA-RegulatoryAffairsSupervisor-BJ
Neural analysis suggests this role is
optimal for Mid+ candidates.
“R&D - GRA - Regulatory Affairs Supervisor - BJ at R&D. Support Line manager for implementing regulatory strategy to obtain the regulatory approval. Support line Manager for the HA interaction for the strategy discussion and be accountable for the HA**** interaction to facilitate the implementation process”
What You'll Achieve.
obtain the regulatory approval; facilitate the implementation process; assure timely and high-quality submission; assure proactive interaction with HA; give timely feedback once there is a query
Industry & Context.
troubleshooting
What You'll Do.
Support Line manager for implementing regulatory strategy to obtain the regulatory approval
Support line Manager for the HA interaction for the strategy discussion and be accountable for the HA**** interaction to facilitate the implementation process
Support line manager for regulatory intelligence collection and analysis
Prepare for the registration submission and approval timeline
Follow up QC testing timely and troubleshooting together with Global technical support
Prepare registration dossier and assure timely and high-quality submission
Follow up closely with registration procedure and assure proactive interaction with HA and give timely feedback once there is a query
Ensure all dossier and information kept on file based on company's requirements
Maintain good relationship with officials and experts
both internal and external
How You'll Work.
Communication Scope
interaction with HA; proactive interaction with HA; give timely feedback; Maintain good relationship with officials and experts
Full Job Description
Support Line manager for implementing regulatory strategy to obtain the regulatory approval · Support line Manager for the HA interaction for the strategy discussion and be accountable for the HA**** interaction to facilitate the implementation process · Support line manager for regulatory intelligence collection and analysis · Prepare for the registration submission and approval timeline · Follow up QC testing timely and troubleshooting together with Global technical support Prepare registration dossier and assure timely and high-quality submission · Follow up closely with registration procedure and assure proactive interaction with HA and give timely feedback once there is a query · Ensure all dossier and information kept on file based on company's requirements Maintain good relationship with officials and experts, both internal and external # 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](https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at [sanofi.com](https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness)!
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