About Human Pharmaceutical Business
With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology and central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demand of Chinese patients.
Responsibilities - Support leader on leading quality and compliance improvement, communicate with - HA or functions for operational effectiveness.
- Ensure process implementation and communication between China RA and BI global team (GRA/GSM etc.).
- Support leader in compliance management and related training
- Centrally coordinate RA project submission and publishing
- China RA Registration dossier archiving management
- Other harmonization work in DRA.
Qualifications - Bachelor’s degree or above, major in Pharmaceutics, Chemistry, Biology and other relevant major
- Good project management skill and experience. Be able to work with a keen sense of urgency and priority.
- Strong learning ability.
- Good personality with team spirit.
- Interpersonal and communication skill.
- >1 years Regulatory Affairs working experiences and project management working experiences in international pharmaceutical companies.
- Regulatory Affairs Project management experiences.