QS Manager

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.

Job Responsibilities:
1. Quality Compliance-Responsible for the adherence to regulatory , cGMP and corporate guideline, especially QS department owned quality system.
2. Be a role model & lead the following the principles of Our Behavios. Coach and develop employees, perform development reviews for QS employees.
3. Responsible for establish，maintain and continuously improve the performance and reliability of site quality system，to ensure the site is in line with GMP compliance.
4. To obey all quality assurance procedure to maintain a high quality level.
5. Maintain and optimize internal and external audit to continues improve the effect and efficiency of quality management；
6. Ensure CRC system is maintained integrate and efficiently in all GMP aspects to further ensure all changes will not cause gap from regulatory compliance.

Requirements：
- Minimum of 5 years' MNC experience of QA
- Good knowledge of GMP
- Familiar with related local regulations
- Pharmacy of relevant
- Good knowledge of related technology, guidelines and standards
- Good audit skill
- Good problem solving skill，communication skill
- Strong leadership