Sr. Regulatory Affairs Supervisor

Department: CMRQ (Clinical Medical Regulatory and Quality)
Location: Beijing

The position

•    Regulatory Planning;
•    Submission and Approvals of New Products and Marketed Products Maintenance;
•    Regional Regulatory Affairs;

•    Regulatory Compliance;
•    Regulatory Influence;
•    Cross functions/Departments Supporting.

Qualifications

•    Bachelor degree or above, majored in Pharmaceutics or related;
•    Have been working for RA position for around 3 years, preferrably with MNCs background;

•    Know drug policies and regulations well;
•    Fluency in both written & spoken English;
•    Team working characteristic;

•    Knowledge of NN mission & vision;
•    Active & creative thinking ability;
•    Strategic thinking.

About the department
In CMRQ, we commit to bringing our products to Chinese market with the fastest speed and top quality, and applying the most scientific way to communicate our products' benefits to our customers. We have 6 team in CMRQ aming to portfolio evaluation and overall strategy; New product approval, Licence maintenance, Product localization; Clinical evidence trial operation Phase (I-IV, NIS); Multiple stakeholders' engagement (HA/KOLs/investigators) and Medical evidence generation/communication.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.