Regulatory Manager Jobs in China

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Regulatory Support Specialist

Labcorp

profile Shanghai - China

Job description - Regulatory Support SpecialistJob Summary:Collection information and prepare the documentation to support the HGRAC application and submission.Provides support and assistance in terms of reviews data for accuracy and compliance to applicable SOPs and regulations. Maintains and expan...

Yesterday
Full Time

Compliance Manager

Thermo Fisher Scientific

profile Shanghai - China

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Compliance Manager - Make an Impact at the Forefront of InnovationThe Clinical Compliance Manager is responsible for the assessment management and reporting of serious breaches of GCP and protocol in cl...

7 days ago
Full Time

Senior Manager, Regulatory Affairs China Immunolog...

Johnson & Johnson

profile Beijing - China

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...

8 days ago
Full Time

Regulatory Affairs Sr. Managerassociate Director

Iqvia

profile Shanghai - China

Essential Functions May act as a Project Manager for a large stand-alone programme involving several regulatory or technical deliverables and/or region and/or operation; Undertakes risk analysis management and contingency plans as appropriate; Provides strategic regulatory and/or technical consultan...

8 days ago
Full Time

Regulatory Affairs Sr. Manager

Amgen

profile Beijing - China

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...

11 days ago
Full Time

Specialist, Regulatory Affairs

Abbvie

profile Beijing - China

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...

22 days ago
Full Time

Regulatory Affairs Manager

Philips

profile Shenzhen - China

Job TitleRegulatory Affairs ManagerJob DescriptionJob Responsibilities: Implements global regulatory strategies and roadmaps by leveraging a comprehensive understanding of the competitive market landscape and product marketing strategy to ensure alignment with organizational objectives. Works under...

22 days ago
Full Time

Senior Regulatory Affairs Manager

Abbott

profile Beijing - China

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...

25 days ago
Full Time

Manager, Apac Regulatory Affairs

Johnson & Johnson

profile Beijing - China

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...

30+ days ago
Full Time

Senior Manager, Apac Regulatory Leader

Johnson & Johnson

profile Beijing - China

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...

30+ days ago
Full Time

Trial Activation Approval Specialist Iii (sr. Cas)

Thermo Fisher Scientific

profile Beijing - China

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...

30+ days ago
Full Time

Trial Activation Approval Specialist Iii (sr. Cas)

Thermo Fisher Scientific

profile Shanghai - China

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...

30+ days ago
Full Time

Startup Lead

Thermo Fisher Scientific

profile Beijing - China

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...

30+ days ago
Full Time

Startup Lead

Thermo Fisher Scientific

profile Shanghai - China

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...

30+ days ago
Full Time

Principal Cas (principal Ssu)

Thermo Fisher Scientific

profile Beijing - China

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....

30+ days ago
Full Time

Principal Cas (principal Ssu)

Thermo Fisher Scientific

profile Shanghai - China

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionDiscover Impactful Work:Manages the preparation review and coordination of Country Submissions in line with global submission strategy.A day in the Life:Prepares reviews and coordinates local regulatory submissions (MoH EC a...

30+ days ago
Full Time

Trial Activation Approval Specialist Iissu Ii

Thermo Fisher Scientific

profile Beijing - China

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...

30+ days ago
Full Time

Regulatory Affairs Manager

Roche

profile Suzhou - China

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

30+ days ago
Full Time

Regulatory Engineering Program Manager

Apple

profile Beijing - China

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...

30+ days ago
Full Time

Quality Conformity Management

Airbus

profile Beijing - China

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...

30+ days ago
Full Time