注册事务经理

Posted 31 Dec 2021

Beijing, Beijing - China

Req Id 237718

Details

 

A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 


Title: Senior Regulatory Affairs Manager / Regulatory Affairs Manager

 

Education: Bachelor degree or above, pharmaceutical or related subject

 

Language: Fluent in English reading, writing and speaking

 

Working experience: More than 5 (RAM) or 8 (SRAM) years regulatory affairs experience in overseas pharmaceutical companies. MNC RA experiences will be appreciated.

 

Main responsibility for this position:

1, To support associate regulatory affair director set up the regulatory strategies’ development for responsible products.

 

2, To give regulatory comments for all activities of related products.

 

3, To communicate with global RA, CMC and manufacturing colleagues to explain Chinese regulation, requirement and RA plans.

 

4, To communicate with authorities to achieve registration objectives.

 

5, To evaluate dossiers provided by global related functions and prepare regulatory dossiers for submission.

 

6, To work together with logistic colleagues to prepare products registration plan to make sure there is no out of stock situation happened.

 

7, To participate RA related organization to share RA voice in these organizations.

 

8, To support associate regulatory affair director in some RA related activities in the company

 

Reporting line: Report to associate regulatory affair director of general medicine product group.


 

What we offer:  With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

 

Curious? Apply and find more information at https://jobs.vibrantm.com

 

Apply Now