Job Information
Boehringer Ingelheim Regulatory Affairs Manager, Operations in Beijing, China
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, the company will launch new medicines or indications in therapeutic areas including CV & metabolism, respiratory, oncology, immunology, CNS and retinal health to meet the demand of Chinese patients.
This position belongs to regulatory affairs department, serving The Chinese Market which encompasses China mainland, Taiwan, Hongkong.
This role requires a detail-oriented professional who can oversee all regulatory affairs and quality assurance activities, ensuring compliance with local and international regulations.
This role drives continuous improvement in regulatory affairs.
Tasks & responsibilities
-Ensure quality management system is well established and implemented in TCM RA.
-Identifies the needs for best practices, processes, SOPs, tools, training sessions and designs related activities. Build systemic processes.
-Collaborate with stakeholders and coordinate with internal teams to ensure regulatory compliance throughout the product lifecycle.
-Provide training and guidance to the team on regulatory and quality matters.
-Participate in continuous improvement initiatives to enhance compliance and streamline processes.
-Ensure TCM RA projects are well planned and status information is systemically tracked.
-Give sufficient operational support to regulatory submissions etc. as needed.
Requirements
-Strong learning ability.
-Good project management skill and experience. Be able to work with a keen sense of urgency and priority.
-Good personalities with team spirit.
-Good interpersonal and communication skills.
-Bachelor degree or above, major in pharmaceutics is preferred.
-At least 7 years related working experiences in regulatory affairs or GxP quality area.
All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.