Regulatory Manager Jobs in Beijing

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

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 (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...

The Program Managers responsibilities include providing comprehensive support for regulatory and quality activities in China and the APAC region. This includes product submissions market initiatives and policy interactions.- Oversee regulatory submissions launch readiness design changes and medical...

Job Description:CONTEXT OF THE POSITIONThis position aims to monitor the quality and compliance system of Airbus Hua ou Training Centre. This includes ensuring compliance with the aviation regulation and Airbus policies related to a training center as well as a simulator operator. The incumbent will...

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...

Job DescriptionPosition title: Manager CMC Regulatory AffairsDepartment: Regulatory AffairsReport to: Associate Director of CMCLocation: Beijing/Shanghai ChinaResponsibilitiesTake CMC lead for products under clinical development and for marketed drug products. Coordinate various aspects of CMC regul...

Are you looking for a role where you can showcase your process improvement skills If so this is the job for you.As Regulatory Affairs Management Professional you will be responsible for leading a process improvement effort across the organization focusing on business alignment cost and cycle time re...