Regulatory Manager Jobs in Beijing

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Career CategoryRegulatoryJob DescriptionRegulatory Affairs Sr. Manager - ChinaReporting to: Head of Regulatory Strategy China RABased in: BeijingJob Description: Develop China registration strategy and implement regulatory submissions (CTN MAA variations) for products within Amgens portfolio in comp...

PurposeDescribe the primary goals objectives or functions or outputs of this position.Coordinate prepare or review regulatory submissions for domestic or international projects.ResponsibilitiesList up to 10 main responsibilities for the job. Include information about the accountability and scope.Pro...

JOB DESCRIPTION:Responsibilities:Collaborate closely with global and local teams to develop and implement regulatory strategies for assigned projects including business development initiatives.Continuously monitor and analyze the regulatory environment in China as well as major global agencies (FD...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionKey responsibilities:Prepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy a...

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionKey responsibilities:Prepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummarized Purpose: Manages the preparation review and coordination of Country Submissions in line with global submission strategy.Key responsibilities:Prepares review and coordinates submissions (MoH EC applications if e.g....

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionPrepares review and coordinates submissions (MoH EC applications if e.g. gene therapy approvals safety dossiers import license) in alignment with global submission strategy.Provides strategy advice (MoH &/or EC) t...