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Senior Manager Regulatory Affairs

• 30+ days ago

Workforce Solutions Virēns Global “ WFS “

Role overview

Qualifications

At least 8-10 years relevant experience
Fluency in English

Responsibilities

Technically and strategically support decision making on DMFs drug development
Compile filing data to obtain CFDA certificates /approvals
Work with stakeholders for follow up and resolution of timely issues
Ensure enhancing Regulatory compliance throughout development and the commercial life cycle
Manage promotional materials review, standard compiling, product labeling, local-test designs, data analysis

Key facts

Remote from: China
Full time
Senior (5-10 years)
Regulatory Affairs Manager
English

Hard skills

Other skills

Packaging And Labeling

About the company

Workforce Solutions Virēns Global “ WFS “

Staffing & Recruiting
Startup
11–50

For open job postings visit workforcesolutionsvirensglobal.com Serving clients in America, Europe, Asia & Australia Recruitment & Advisory Support to Core Business & Support Business Corporate Functions - Strategic Management, Accounting & Finance, Technology & Process Development, General Management , Human Resource Management, Legal , Planning, Public & Government Relations, Product & Service Development, Marketing, Sales & Customer Support, Operations & Procurement We provide Recruitment and Staffing and Employment advisory services including support in drafting contracts, policies, contracts administration and recruitment administration. We partner with recruitment consultants and legal advisors to execute end to end recruitment administration. Our code of practices: compliance with consumer protection act compliance with fair competition act compliance with wage equity principals

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Job description

Senior Manager Regulatory Affair

A well-known large healthcare company is hiring for Senior Manager Regulatory Affairs to implement CFDA registration projects, make strategy for product line and DMFs and Drug Product applications.. Responsibilities include:

Technically and strategically support decision making on DMFs & drug development
Compile filing data to obtain CFDA certificates /approvals
Work with stakeholders for follow up and resolution of timely issues
Ensure enhancing Regulatory compliance throughout development and the commercial life cycle
Manage other stuff like promotional materials review, standard compiling, product labeling, local-test designs, data analysis

Requirements

Atleast 8-10 years relevant experience
Fluency in English

If you are interested in the above opportunity please apply. Only relevant candidates will be contacted.

workforcesolutionsvirensglobal... Locations: America, Europe, Asia & Australia

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