KEY RESPONSIBILUTIES:
1. The incumbent will provide legal support for CSL Behring’s operations and manufacturing activities in China, including but not limited to Wuhan.
2. Review, draft and negotiate all contracts required by the plasma collection centers in China as well as the Wuhan fractionation site in the conduct of its business (except those which are the responsibility of Legal Services) subject to CSL’s Legal Policy, including R&D, plasma collection, fractionation, purchase and sale, distribution, agency, consulting, services, tender consulting, supply and install, construction management and master services agreements.
3. Advise clients on legal issues related to CSL Behring’s plasma collection, manufacturing, and operational activities in China.
4. Supervise and manage litigation and litigation exposure to protect the interests of CSL Behring’s operations, in consultation with the Head of Legal, China.
5. Learn, become familiar with, and stay informed on relevant legal and health care issues to proactively inform clients and help them anticipate and prepare for changes in the health care environment that may materially impact the business.
6. Partner with Business Integrity & Risk to help ensure business processes and activities are and remain in compliance with applicable laws, regulations, and company policies, and to maintain open and effective avenues of communication among Legal, Business Integrity & Risk and the business.
7. Serve as an escalation point for Legal Services in relation to agreements within their area of responsibility that are required by the plasma collection centers in China as well as the Wuhan fractionation site.
8. Support related client groups including Engineering, Procurement, Manufacturing, Supply Chain, Human Resources, Finance, Business Technology and Regulatory Affairs, including coordinating legal advice on a global basis.
9. Develop and deliver training on legal matters as required or requested.
10. Coordinate work with outside counsel as appropriate or assigned.
11. Establish and build good working relationships with internal clients based on mutual trust and respect and knowledge of the company’s business and its needs and goals.


ESSENTIAL CRITERIA:
1. Law degree or professional legal qualification
2. Deep and demonstrable experience (minimum of 5 years), with some demonstrated experience in supporting a manufacturing, pharmaceutical or medical device company, either as in-house or external counsel
3. Strong understanding of laws, regulations and industry guidance related to the pharmaceutical industry
4. Self-motivated, self-starter, results oriented
5. Ability to work in a cross-functional, cross-cultural matrixed environment

其他信息

行业要求：全部行业