上海招聘

US Pharmacopeia-China	Job Title:	Sr. Director, Chemicals
Job Description	Reports to:	Vice President and General Manager, China Operations

Function of the Position:

This is a key scientific leadership role which is responsible for overseeing the all the activities under Chemicals such as Reference Standard Collaborative Activities and Analytical Research and Development (ARD) activities in the areas of Chemical Medicines, Excipients and Foods. ARD activities involve documentary standards development, which includes analytical method development and analytical method validation and also Characterization. This requires to manage all daily operations of all the Chemical Laboratories. Contribute to the credibility and enforceability of USP-NF Modernization by establishing a science-based culture of quality and productivity. Provide support to development and revision of documentary standards for Drug Substances and products for the USP-NF and for the development and evaluation of the associated USP Reference Standards.

Roles and responsibilities:

• Responsible for ensuring that laboratories and scientists are aligned with the mission, vision, objectives, and business strategy of the organization. Manage laboratory activities related to standard setting in pharmaceuticals, excipients, dietary supplements and food ingredients


• Directs efforts of the laboratory in USP Reference Materials development and Analytical Methods and validation development and characterization .


• Develops and implements research and development strategies and program definition subject to USP expert committees’ policies through coordination with Scientific Liaisons and USP Headquarter, Rockville, MD, USA.

• Coordinates technical support with the headquarter for the USP-NF, food and USP reference standards in China.

• Develops and manages annual budgets, and projects resources, capital, personnel needs for the organization, and operation and maintenance of Chemical laboratories. Ensures that the laboratories are staffed appropriately and that all personnel are managed, trained and developed according to USP practices, policies and core values and that meet the needs of the business.


• Provides effective leadership to drive laboratory productivity, achieve timelines, while maintaining a high level of quality output.


• Participates on expert committees and task forces for strategic planning of the organization


• Responsible for ensuring that all SOPs, Protocols, reports are prepared properly, implemented and communicated effectively, and followed compliantly.


• Champion all initiatives related to ISO-9001 & ISO-17025 recertification process. Engage staff and ensure relevant staff is knowledgeable and understands the Quality Management Systems.


• Teach USP Pharmacopeial Education at training classes as assigned appropriately.


• Performs other related duties as required.

Minimum Requirements:

Ph.D. in chemistry or related field with about 15 years of working experience in the field of QC, analytical research and development, includes analytical method development and validation. Must have at least 5 years of experience in a senior position or other equivalent leadership role. . Must have experience with implementing and maintaining a GMP/GLP environment including knowledge of documentation procedures. Must have hands on experience in guiding a teams of chemists who handles various sophisticated analytical instruments like HPLC, GC, FTIR, UV-Visible etc. Evidence of success in the leadership and management of scientific research. Must be fluent in English and Chinese.

KSAs and Training and Experience:

Must be familiar with USP/NF. Excellent interpersonal skills, ability to develop important relationships with customers and key stakeholders. Demonstrated proficiency in leadership, management and staff development practices, tools, and methodology. Broad experience for research and development labs, in a multinational pharmaceutical company is desirable. Having prior experience in setting-up new laboratory and thorough knowledge in implementing Quality Management Systems or QA is desirable.

Frequent Contacts

USP Headquarters and other USP internal laboratories

Supervisory Requirements:

Director, Reference Standards Lab

Director, USP-NF Modernization Lab

Director, Food Lab

Manager, Lab Operations

Scientific Liaison

Status:

Exempt

除美国之外，USP标准和标准品在的世界上其他130多个国家也得到广泛的使用。建立185年以来，这些标准一直服务于世界各地，确保公众获得优质的药品。
鉴于中国和亚太地区其他国家的战略重要性，USP在上海张江高科技园区设立了中华区总部，并建成了USP在全球的第三个标准品研发中心实验室。现公开招聘所述职位，诚邀您的加盟。
应聘者请将中英文简历、近照、应聘职位和期望薪资发送给我们。
欲了解USP更多详情，欢迎访问我们的网站。
请将中英文简历发至所述邮箱: uspchinahr@usp.org

The United States Pharmacopoeia(USP)is the official standards-setting authority for all prescription and over-the-counter medicines, dietary supplements, and other healthcare products manufactured and sold in the United States.USP is also a world leader and its reference standards are recognized and used in many other countries outside the United States. These standards have been helping to ensure good pharmaceutical care for people throughout the world for more than 185 years.
For more details about USP, please visit our website.
Attaching great importance to China and Asian Pacific countries, USP is setting up its regional headquarter in Shanghai located in Zhang Jiang Hi-Tech Park.
Currently we are looking for the positions for USP-China.Please indicate the position that you are interested and send us your resume and salary expectation to us.
Please send your bilingual resume to us
请将中英文简历发至所述邮箱: uspchinahr@usp.org